Multivalent and multispecific gitr-binding fusion proteins

ABSTRACT

This disclosure generally provides molecules that specifically engage glucocorticoid-induced TNFR-related protein (GITR), a member of the TNF receptor superfamily (TNFRSF). More specifically, the disclosure relates to multivalent and/or multispecific molecules that bind at least GITR.

RELATED APPLICATIONS

This application is a continuation of U.S. patent application Ser. No. 15/217,754, filed Jul. 22, 2016, which claims the benefit of U.S. Provisional Application No. 62/195,822, filed Jul. 23, 2015, the contents of each of which are incorporated herein by reference in their entirety.

INCORPORATION OF SEQUENCE LISTING

The contents of the text file named “INHI022C01USSeqList,” which was created on Jun. 9, 2017 and is 209 KB in size, are hereby incorporated by reference in their entirety.

FIELD OF THE INVENTION

This disclosure generally provides molecules that specifically engage glucocorticoid-induced TNFR-related protein (GITR), a member of the TNF receptor superfamily (TNFRSF). More specifically, the disclosure relates to multivalent and/or multispecific molecules that bind at least GITR.

BACKGROUND OF THE INVENTION

The tumor necrosis factor receptor superfamily consists of several structurally related cell surface receptors. Activation by multimeric ligands is a common feature of many of these receptors. Many members of the TNFRSF have therapeutic utility in numerous pathologies, if activated properly. Importantly, to properly agonize this receptor family often requires higher order clustering, and conventional bivalent antibodies are not ideal for this. Therefore, there exists a therapeutic need for more potent agonist molecules of the TNFRSF.

SUMMARY OF THE INVENTION

The disclosure provides multivalent TNF receptor superfamily (TNFRSF) binding fusion polypeptides that bind at least glucocorticoid-induced TNFR-related protein (GITR, also known as tumor necrosis factor receptor superfamily member 18 (TNFRSF 18) and/or activation-inducible TNFR family receptor (AITR)). These molecules that bind at least GITR are referred to herein as “GITR-targeting molecules” or “GITR-targeting fusions” or “GITR-targeting proteins” or “GITR-targeting fusion polypeptides” or “GITR-targeting fusion proteins.” In some embodiments, the GITR-targeting molecule is a multivalent molecule, for example, a multivalent GITR-targeting fusion protein. In some embodiments, the GITR-targeting molecule is a multispecific molecule, for example, a multispecific GITR-targeting fusion protein. In some embodiments, the GITR-targeting molecule is a multivalent and multispecific molecule, for example, a multivalent and multispecific GITR-targeting fusion protein. As used herein, the term “fusion protein” or “fusion polypeptide” or “GITR-targeting fusion protein” or “GITR-targeting fusion polypeptide,” unless otherwise specifically denoted, refers to any fusion protein embodiment of the disclosure, including, but not limited to, multivalent fusion proteins, multispecific fusion proteins, or multivalent and multispecific fusion proteins.

These GITR-targeting molecules include at least one domain that binds GITR, referred to herein as a “GITR-binding domain” (GITR-BD). These GITR-BDs include a polypeptide sequence that specifically binds to GITR. In some embodiments, the GITR-BD includes a polypeptide sequence that is or is derived from an antibody or antibody fragment including, for example, scFv, Fabs, single domain antibodies (sdAb), V_(NAR), or VHHs. In some embodiments, the GITR-BD includes a human or humanized sdAb.

The GITR-targeting molecules of the disclosure overcome problems and limitations from convention antibodies that target members of the TNF receptor superfamily (TNFRSF), including GITR. Conventional antibodies targeting members of the TNFRSF have been shown to require an exogenous crosslinking to achieve sufficient agonist activity, as evidenced by the necessity for Fc-gamma Receptor (FcγRs) for the activity antibodies to DR4, DR5, GITR and OX40 (Ichikawa et al 2001 al Nat. Med. 7, 954-960, Li et al 2008 Drug Dev. Res. 69, 69-82; Pukac et al 2005 Br. J. Cancer 92, 1430-1441; Yanda et al 2008 Ann. Oncol. 19, 1060-1067; Yang et al 2007 Cancer Lett. 251:146-157; Bulliard et al 2013 JEM 210(9): 1685; Bulliard et al 2014 Immunol and Cell Biol 92: 475-480). In addition to crosslinking via FcγRs other exogenous agents including addition of the oligomeric ligand or antibody binding entities (e.g. protein A and secondary antibodies) have be demonstrated to enhance anti-TNFRSF antibody clustering and downstream signaling. For example, the addition of the DR5 ligand TRAIL enhanced the apoptosis inducing ability of an anti-DR5 antibody (Graves et al 2014 Cancer Cell 26: 177-189). These findings suggest the need for clustering of TNFRSFs beyond a dimer.

The present disclosure provides isolated polypeptides that specifically bind GITR. In some embodiments, the isolated polypeptide is derived from antibodies or antibody fragments including scFv, Fabs, single domain antibodies (sdAb), V_(NAR), or VHHs. In some embodiments, the isolated polypeptide is human or humanized sdAb. The sdAb fragments can be derived from VHH, V_(NAR), engineered VH or VK domains. VHHs can be generated from camelid heavy chain only antibodies. V_(NAR) can be generated from cartilaginous fish heavy chain only antibodies. Various methods have been implemented to generate monomeric sdAbs from conventionally heterodimeric VH and VK domains, including interface engineering and selection of specific germline families. In other embodiments, the isolated polypeptides are derived from non-antibody scaffold proteins for example but not limited to designed ankyrin repeat proteins (darpins), avimers, anticalin/lipocalins, centyrins and fynomers.

In some embodiments, the isolated polypeptide includes an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80. In some embodiments, the isolated polypeptide includes an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62. In some embodiments, the isolated polypeptide includes an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80.

In some embodiments, the isolated polypeptide includes an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80. In some embodiments, the isolated polypeptide includes an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62. In some embodiments, the isolated polypeptide includes an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80.

In some embodiments, the isolated polypeptide comprises a complementarity determining region 1 (CDR1) comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 106, 109, 112, 117, 120, 125, 131, 138, 143, 148, and 149; a complementarity determining region 2 (CDR2) comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 107, 110, 113, 115, 118, 121, 123, 128, 130, 132, 134, 136, 137, 139, 141, 144, and 147; and a complementarity determining region 3 (CDR3) comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 108, 111, 114, 116, 119, 122, 124, 126, 127, 129, 133, 135, 140, 142, 145, 146, and 150.

The present disclosure also provides multivalent TNFRSF binding fusion proteins, which comprise two or more TNFRSF binding domains (TBDs), where at least one TBD binds GITR, referred to herein as a GITR-binding domain (GITR-BD). In some embodiments, the fusion proteins of the present disclosure have utility in treating neoplasms. In some embodiments, the fusion proteins of the present disclosure bind TNFRSF member expressed on a tumor cell, for example, at least GITR.

In some embodiments, GITR-BDs of the present disclosure are derived from antibodies or antibody fragments including scFv, Fabs, single domain antibodies (sdAb), V_(NAR), or VHHs. In some embodiments, the GITR-BDs are human or humanized sdAb. The sdAb fragments can be derived from VHH, V_(NAR), engineered VH or VK domains. VHHs can be generated from camelid heavy chain only antibodies. V_(NAR)s can be generated from cartilaginous fish heavy chain only antibodies. Various methods have been implemented to generate monomeric sdAbs from conventionally heterodimeric VH and VK domains, including interface engineering and selection of specific germline families. In other embodiments, the GITR-BDs are derived from non-antibody scaffold proteins for example but not limited to designed ankyrin repeat proteins (darpins), avimers, anticalin/lipocalins, centyrins and fynomers.

Generally, the multivalent fusion proteins of the present disclosure include at least two or more GITR-BDs operably linked via a linker polypeptide. The utilization of sdAb fragments as the specific GITR-BD sequences within the multivalent fusion proteins of the present disclosure has the benefit of avoiding the heavy chain:light chain mis-pairing problem common to many bi/multispecific antibody approaches. In addition, the multivalent fusion proteins of the present disclosure avoid the use of long linkers necessitated by many bispecific antibodies.

In some embodiments, the multivalent fusion protein contains two or more different GITR-BDs. In some embodiments, the multivalent fusion protein contains three or more different GITR-BDs. In some embodiments, the multivalent fusion protein contains four or more different GITR-BDs. In some embodiments, the multivalent fusion protein contains five or more different GITR-BDs. In some embodiments, the multivalent fusion protein contains six or more different GITR-BDs.

In some embodiments, the multivalent fusion protein contains multiple copies of a GITR-BD. For example, in some embodiments, the multivalent fusion protein contains at least two copies of a GITR-BD. In some embodiments, the multivalent fusion protein contains at least three copies of a GITR-BD. In some embodiments, the multivalent fusion protein contains at least four copies of a GITR-BD. In some embodiments, the multivalent fusion protein contains at least five copies of a GITR-BD. In some embodiments, the multivalent fusion protein contains at least six copies of a GITR-BD. In some embodiments, the multivalent fusion protein contains six or more copies of a GITR-BD.

In some embodiments, the multivalent fusion protein contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80. In some embodiments, the multivalent fusion protein contains two or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80. In some embodiments, the multivalent fusion protein contains three or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80. In some embodiments, the multivalent fusion protein contains four or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80. In some embodiments, the multivalent fusion protein contains five or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80. In some embodiments, the multivalent fusion protein contains six or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80.

In some embodiments, the multivalent fusion protein contains at least one GITR-BD that comprises an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80. In some embodiments, the multivalent fusion protein contains two or more copies of a GITR-BD that comprises an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80. In some embodiments, the multivalent fusion protein contains three or more copies of a GITR-BD that comprises an amino acid sequence that is at least 50%, 60%, 65%, 700, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80. In some embodiments, the multivalent fusion protein contains four or more copies of a GITR-BD that comprises an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80. In some embodiments, the multivalent fusion protein contains five or more copies of a GITR-BD that comprises an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80. In some embodiments, the multivalent fusion protein contains six or more copies of a GITR-BD that comprises an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80.

In some embodiments, the multivalent fusion protein contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62. In some embodiments, the multivalent fusion protein contains two or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62. In some embodiments, the multivalent fusion protein contains three or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62. In some embodiments, the multivalent fusion protein contains four or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62. In some embodiments, the multivalent fusion protein contains five or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62. In some embodiments, the multivalent fusion protein contains six or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62.

In some embodiments, the multivalent fusion protein contains at least one GITR-BD that comprises an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62. In some embodiments, the multivalent fusion protein contains two or more copies of a GITR-BD that comprises an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62. In some embodiments, the multivalent fusion protein contains three or more copies of a GITR-BD that comprises an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62. In some embodiments, the multivalent fusion protein contains four or more copies of a GITR-BD that comprises an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62. In some embodiments, the multivalent fusion protein contains five or more copies of a GITR-BD that comprises an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62. In some embodiments, the multivalent fusion protein contains six or more copies of a GITR-BD that comprises an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62.

In some embodiments, the multivalent fusion protein contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80. In some embodiments, the multivalent fusion protein contains two or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80. In some embodiments, the multivalent fusion protein contains three or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80. In some embodiments, the multivalent fusion protein contains four or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80. In some embodiments, the multivalent fusion protein contains five or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80. In some embodiments, the multivalent fusion protein contains six or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80.

In some embodiments, the multivalent fusion protein contains at least one GITR-BD that comprises an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80. In some embodiments, the multivalent fusion protein contains two or more copies of a GITR-BD that comprises an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80. In some embodiments, the multivalent fusion protein contains three or more copies of a GITR-BD that comprises an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80. In some embodiments, the multivalent fusion protein contains four or more copies of a GITR-BD that comprises an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80. In some embodiments, the multivalent fusion protein contains five or more copies of a GITR-BD that comprises an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80. In some embodiments, the multivalent fusion protein contains six or more copies of a GITR-BD that comprises an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80.

In some embodiments, the multivalent fusion protein contains at least one GITR-BD that comprises a complementarity determining region 1 (CDR1) comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 106, 109, 112, 117, 120, 125, 131, 138, 143, 148, and 149; a complementarity determining region 2 (CDR2) comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 107, 110, 113, 115, 118, 121, 123, 128, 130, 132, 134, 136, 137, 139, 141, 144, and 147; and a complementarity determining region 3 (CDR3) comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 108, 111, 114, 116, 119, 122, 124, 126, 127, 129, 133, 135, 140, 142, 145, 146, and 150. In some embodiments, the multivalent fusion protein contains two or more copies of a GITR-BD that comprises a CDR1 comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 106, 109, 112, 117, 120, 125, 131, 138, 143, 148, and 149; a CDR2 comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 107, 110, 113, 115, 118, 121, 123, 128, 130, 132, 134, 136, 137, 139, 141, 144, and 147; and a CDR3 comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 108, 111, 114, 116, 119, 122, 124, 126, 127, 129, 133, 135, 140, 142, 145, 146, and 150. In some embodiments, the multivalent fusion protein contains three or more copies of a GITR-BD that comprises a CDR1 comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 106, 109, 112, 117, 120, 125, 131, 138, 143, 148, and 149; a CDR2 comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 107, 110, 113, 115, 118, 121, 123, 128, 130, 132, 134, 136, 137, 139, 141, 144, and 147; and a CDR3 comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 108, 111, 114, 116, 119, 122, 124, 126, 127, 129, 133, 135, 140, 142, 145, 146, and 150. In some embodiments, the multivalent fusion protein contains four or more copies of a GITR-BD that comprises a CDR1 comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 106, 109, 112, 117, 120, 125, 131, 138, 143, 148, and 149; a CDR2 comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 107, 110, 113, 115, 118, 121, 123, 128, 130, 132, 134, 136, 137, 139, 141, 144, and 147; and a CDR3 comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 108, 111, 114, 116, 119, 122, 124, 126, 127, 129, 133, 135, 140, 142, 145, 146, and 150. In some embodiments, the multivalent fusion protein contains five or more copies of a GITR-BD that comprises a CDR1 comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 106, 109, 112, 117, 120, 125, 131, 138, 143, 148, and 149; a CDR2 comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 107, 110, 113, 115, 118, 121, 123, 128, 130, 132, 134, 136, 137, 139, 141, 144, and 147; and a CDR3 comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 108, 111, 114, 116, 119, 122, 124, 126, 127, 129, 133, 135, 140, 142, 145, 146, and 150. In some embodiments, the multivalent fusion protein contains six or more copies of a GITR-BD that comprises a CDR1 comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 106, 109, 112, 117, 120, 125, 131, 138, 143, 148, and 149; a CDR2 comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 107, 110, 113, 115, 118, 121, 123, 128, 130, 132, 134, 136, 137, 139, 141, 144, and 147; and a CDR3 comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 108, 111, 114, 116, 119, 122, 124, 126, 127, 129, 133, 135, 140, 142, 145, 146, and 150.

In some embodiments, the multivalent fusion protein contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6. In some embodiments, the multivalent fusion protein contains two or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6. In some embodiments, the multivalent fusion protein contains three or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6. In some embodiments, the multivalent fusion protein contains four or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6. In some embodiments, the multivalent fusion protein contains five or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6. In some embodiments, the multivalent fusion protein contains six or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6.

In some embodiments, the multivalent fusion protein contains at least one GITR-BD that comprises an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6. In some embodiments, the multivalent fusion protein contains two or more copies of a GITR-BD that comprises an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6. In some embodiments, the multivalent fusion protein contains three or more copies of a GITR-BD that comprises an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6. In some embodiments, the multivalent fusion protein contains four or more copies of a GITR-BD that comprises an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6. In some embodiments, the multivalent fusion protein contains five or more copies of a GITR-BD that comprises an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6. In some embodiments, the multivalent fusion protein contains six or more copies of a GITR-BD that comprises an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6.

In some embodiments, the multivalent fusion protein contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6. In some embodiments, the multivalent fusion protein contains two or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6. In some embodiments, the multivalent fusion protein contains three or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6. In some embodiments, the multivalent fusion protein contains four or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6. In some embodiments, the multivalent fusion protein contains five or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6. In some embodiments, the multivalent fusion protein contains six or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6.

In some embodiments, the multivalent fusion protein contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 1. In some embodiments, the multivalent fusion protein contains two or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 1. In some embodiments, the multivalent fusion protein contains three or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 1. In some embodiments, the multivalent fusion protein contains four or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 1. In some embodiments, the multivalent fusion protein contains five or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 1. In some embodiments, the multivalent fusion protein contains six or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 1.

In some embodiments, the multivalent fusion protein contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 2. In some embodiments, the multivalent fusion protein contains two or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 2. In some embodiments, the multivalent fusion protein contains three or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 2. In some embodiments, the multivalent fusion protein contains four or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 2. In some embodiments, the multivalent fusion protein contains five or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 2. In some embodiments, the multivalent fusion protein contains six or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 2.

In some embodiments, the multivalent fusion protein contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 3. In some embodiments, the multivalent fusion protein contains two or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 3. In some embodiments, the multivalent fusion protein contains three or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 3. In some embodiments, the multivalent fusion protein contains four or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 3. In some embodiments, the multivalent fusion protein contains five or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 3. In some embodiments, the multivalent fusion protein contains six or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 3.

In some embodiments, the multivalent fusion protein contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 4. In some embodiments, the multivalent fusion protein contains two or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 4. In some embodiments, the multivalent fusion protein contains three or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 4. In some embodiments, the multivalent fusion protein contains four or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 4. In some embodiments, the multivalent fusion protein contains five or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 4. In some embodiments, the multivalent fusion protein contains six or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 4.

In some embodiments, the multivalent fusion protein contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 5. In some embodiments, the multivalent fusion protein contains two or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 5. In some embodiments, the multivalent fusion protein contains three or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 5. In some embodiments, the multivalent fusion protein contains four or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 5. In some embodiments, the multivalent fusion protein contains five or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 5. In some embodiments, the multivalent fusion protein contains six or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 5.

In some embodiments, the multivalent fusion protein contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 6. In some embodiments, the multivalent fusion protein contains two or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 6. In some embodiments, the multivalent fusion protein contains three or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 6. In some embodiments, the multivalent fusion protein contains four or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 6. In some embodiments, the multivalent fusion protein contains five or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 6. In some embodiments, the multivalent fusion protein contains six or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 6.

In some embodiments, the multivalent fusion protein contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6. In some embodiments, the multivalent fusion protein contains two or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6. In some embodiments, the multivalent fusion protein contains three or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6. In some embodiments, the multivalent fusion protein contains four or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6. In some embodiments, the multivalent fusion protein contains five or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6. In some embodiments, the multivalent fusion protein contains six or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6.

In some embodiments, the multivalent fusion protein contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 1. In some embodiments, the multivalent fusion protein contains two or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 1. In some embodiments, the multivalent fusion protein contains three or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 1. In some embodiments, the multivalent fusion protein contains four or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 1. In some embodiments, the multivalent fusion protein contains five or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 1. In some embodiments, the multivalent fusion protein contains six or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 1.

In some embodiments, the multivalent fusion protein contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 2. In some embodiments, the multivalent fusion protein contains two or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 2. In some embodiments, the multivalent fusion protein contains three or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 2. In some embodiments, the multivalent fusion protein contains four or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 2. In some embodiments, the multivalent fusion protein contains five or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 2. In some embodiments, the multivalent fusion protein contains six or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 2.

In some embodiments, the multivalent fusion protein contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 3. In some embodiments, the multivalent fusion protein contains two or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 3. In some embodiments, the multivalent fusion protein contains three or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 3. In some embodiments, the multivalent fusion protein contains four or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 3. In some embodiments, the multivalent fusion protein contains five or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 3. In some embodiments, the multivalent fusion protein contains six or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 3.

In some embodiments, the multivalent fusion protein contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 4. In some embodiments, the multivalent fusion protein contains two or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 4. In some embodiments, the multivalent fusion protein contains three or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 4. In some embodiments, the multivalent fusion protein contains four or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 4. In some embodiments, the multivalent fusion protein contains five or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 4. In some embodiments, the multivalent fusion protein contains six or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 4.

In some embodiments, the multivalent fusion protein contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 5. In some embodiments, the multivalent fusion protein contains two or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 5. In some embodiments, the multivalent fusion protein contains three or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 5. In some embodiments, the multivalent fusion protein contains four or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 5. In some embodiments, the multivalent fusion protein contains five or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 5. In some embodiments, the multivalent fusion protein contains six or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 5.

In some embodiments, the multivalent fusion protein contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 6. In some embodiments, the multivalent fusion protein contains two or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 6. In some embodiments, the multivalent fusion protein contains three or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 6. In some embodiments, the multivalent fusion protein contains four or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 6. In some embodiments, the multivalent fusion protein contains five or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 6. In some embodiments, the multivalent fusion protein contains six or more copies of a GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising the amino acid sequence of SEQ ID NO: 6.

In some embodiments, the multivalent fusion protein contains at least one GITR-BD that comprises a complementarity determining region 1 (CDR1) comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 106, 109, 112, 117, 120, 125, 131, 138, 143, 148, and 149; a complementarity determining region 2 (CDR2) comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 107, 110, 113, 115, 118, 121, 123, 128, 130, 132, 134, 136, 137, 139, 141, 144, and 147; and a complementarity determining region 3 (CDR3) comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 108, 111, 114, 116, 119, 122, 124, 126, 127, 129, 133, 135, 140, 142, 145, 146, and 150 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6. In some embodiments, the multivalent fusion protein contains two or more copies of a GITR-BD that comprises a CDR1 comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 106, 109, 112, 117, 120, 125, 131, 138, 143, 148, and 149; a CDR2 comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 107, 110, 113, 115, 118, 121, 123, 128, 130, 132, 134, 136, 137, 139, 141, 144, and 147; and a CDR3 comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 108, 111, 114, 116, 119, 122, 124, 126, 127, 129, 133, 135, 140, 142, 145, 146, and 150 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6. In some embodiments, the multivalent fusion protein contains three or more copies of a GITR-BD that comprises a CDR1 comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 106, 109, 112, 117, 120, 125, 131, 138, 143, 148, and 149; a CDR2 comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 107, 110, 113, 115, 118, 121, 123, 128, 130, 132, 134, 136, 137, 139, 141, 144, and 147; and a CDR3 comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 108, 111, 114, 116, 119, 122, 124, 126, 127, 129, 133, 135, 140, 142, 145, 146, and 150 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6. In some embodiments, the multivalent fusion protein contains four or more copies of a GITR-BD that comprises a CDR1 comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 106, 109, 112, 117, 120, 125, 131, 138, 143, 148, and 149; a CDR2 comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 107, 110, 113, 115, 118, 121, 123, 128, 130, 132, 134, 136, 137, 139, 141, 144, and 147; and a CDR3 comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 108, 111, 114, 116, 119, 122, 124, 126, 127, 129, 133, 135, 140, 142, 145, 146, and 150 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6. In some embodiments, the multivalent fusion protein contains five or more copies of a GITR-BD that comprises a CDR1 comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 106, 109, 112, 117, 120, 125, 131, 138, 143, 148, and 149; a CDR2 comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 107, 110, 113, 115, 118, 121, 123, 128, 130, 132, 134, 136, 137, 139, 141, 144, and 147; and a CDR3 comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 108, 111, 114, 116, 119, 122, 124, 126, 127, 129, 133, 135, 140, 142, 145, 146, and 150 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6. In some embodiments, the multivalent fusion protein contains six or more copies of a GITR-BD that comprises a CDR1 comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 106, 109, 112, 117, 120, 125, 131, 138, 143, 148, and 149; a CDR2 comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 107, 110, 113, 115, 118, 121, 123, 128, 130, 132, 134, 136, 137, 139, 141, 144, and 147; and a CDR3 comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 108, 111, 114, 116, 119, 122, 124, 126, 127, 129, 133, 135, 140, 142, 145, 146, and 150 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6.

In some embodiments, the multivalent fusion protein comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 81-105. In some embodiments, the multivalent fusion protein comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 81-93. In some embodiments, the multivalent fusion protein comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 94-105.

In some embodiments, the multivalent fusion protein comprises an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 81-105. In some embodiments, the multivalent fusion protein comprises an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 81-93. In some embodiments, the multivalent fusion protein comprises an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 94-105.

In some embodiments, the multivalent fusion protein comprises the amino acid sequence of SEQ ID NO: 81. In some embodiments, the multivalent fusion protein comprises the amino acid sequence of SEQ ID NO: 82. In some embodiments, the multivalent fusion protein comprises the amino acid sequence of SEQ ID NO: 83. In some embodiments, the multivalent fusion protein comprises the amino acid sequence of SEQ ID NO: 84. In some embodiments, the multivalent fusion protein comprises the amino acid sequence of SEQ ID NO: 85. In some embodiments, the multivalent fusion protein comprises the amino acid sequence of SEQ ID NO: 86. In some embodiments, the multivalent fusion protein comprises the amino acid sequence of SEQ ID NO: 87. In some embodiments, the multivalent fusion protein comprises the amino acid sequence of SEQ ID NO: 88. In some embodiments, the multivalent fusion protein comprises the amino acid sequence of SEQ ID NO: 89. In some embodiments, the multivalent fusion protein comprises the amino acid sequence of SEQ ID NO: 90. In some embodiments, the multivalent fusion protein comprises the amino acid sequence of SEQ ID NO: 91. In some embodiments, the multivalent fusion protein comprises the amino acid sequence of SEQ ID NO: 92. In some embodiments, the multivalent fusion protein comprises the amino acid sequence of SEQ ID NO: 93. In some embodiments, the multivalent fusion protein comprises the amino acid sequence of SEQ ID NO: 94. In some embodiments, the multivalent fusion protein comprises the amino acid sequence of SEQ ID NO: 95. In some embodiments, the multivalent fusion protein comprises the amino acid sequence of SEQ ID NO: 96. In some embodiments, the multivalent fusion protein comprises the amino acid sequence of SEQ ID NO: 97. In some embodiments, the multivalent fusion protein comprises the amino acid sequence of SEQ ID NO: 98. In some embodiments, the multivalent fusion protein comprises the amino acid sequence of SEQ ID NO: 99. In some embodiments, the multivalent fusion protein comprises the amino acid sequence of SEQ ID NO: 100. In some embodiments, the multivalent fusion protein comprises the amino acid sequence of SEQ ID NO: 101. In some embodiments, the multivalent fusion protein comprises the amino acid sequence of SEQ ID NO: 102. In some embodiments, the multivalent fusion protein comprises the amino acid sequence of SEQ ID NO: 103. In some embodiments, the multivalent fusion protein comprises the amino acid sequence of SEQ ID NO: 104. In some embodiments, the multivalent fusion protein comprises the amino acid sequence of SEQ ID NO: 105.

In some embodiments, the multivalent GITR-targeting fusion protein is tetravalent. As used herein, a tetravalent GITR-targeting molecule refers to two copies of a GITR-targeting fusion protein that includes two GITR-BDs. For example, in some embodiments, a tetravalent GITR-targeting molecule of the disclosure includes two copies of a GITR-targeting fusion protein having the following structure: (GITR-BD)-Linker-(GITR-BD)-Linker-Hinge-Fc. In some embodiments, the tetravalent GITR-targeting molecule of the disclosure includes two copies of a GITR-binding fusion protein having the following structure: (GITR-BD)-Linker-(GITR-BD)-Linker-Hinge-Fc, where the GITR-BD is an isolated polypeptide sequence that binds GITR. In some embodiments, the tetravalent GITR-targeting molecule of the disclosure includes two copies of a GITR-binding fusion protein having the following structure: (GITR-BD)-Linker-(GITR-BD)-Linker-Hinge-Fc, where the GITR-BD is an sdAb sequence that binds GITR. In some embodiments, the tetravalent GITR-targeting molecule of the disclosure includes two copies of a GITR-binding fusion protein having the following structure: (GITR-BD)-Linker-(GITR-BD)-Linker-Hinge-Fc, where the GITR-BD is a humanized or fully human sdAb sequence that binds GITR. In some embodiments, the GITR-BD comprises a complementarity determining region 1 (CDR1) comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 106, 109, 112, 117, 120, 125, 131, 138, 143, 148, and 149; a complementarity determining region 2 (CDR2) comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 107, 110, 113, 115, 118, 121, 123, 128, 130, 132, 134, 136, 137, 139, 141, 144, and 147; and a complementarity determining region 3 (CDR3) comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 108, 111, 114, 116, 119, 122, 124, 126, 127, 129, 133, 135, 140, 142, 145, 146, and 150. In some embodiments, the tetravalent GITR-targeting molecule contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80. In some embodiments, the tetravalent GITR-targeting molecule contains at least one GITR-BD that comprises an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80. In some embodiments, the tetravalent GITR-targeting molecule contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62. In some embodiments, the tetravalent GITR-targeting molecule contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80. In some embodiments, the tetravalent GITR-targeting molecule comprises two copies of an amino acid sequence selected from the group consisting of SEQ ID NO: 81-93.

In some embodiments, the multivalent GITR-targeting fusion protein is hexavalent. As used herein, a hexavalent GITR-targeting molecule refers to two copies of a GITR-targeting fusion protein that includes three GITR-BDs. For example, in some embodiments, a hexavalent GITR-targeting molecule of the disclosure includes two copies of a GITR-targeting fusion protein having the following structure: (GITR-BD)-Linker-(GITR-BD)-Linker-(GITR-BD)-Linker-Hinge-Fc. In some embodiments, the hexavalent GITR-targeting molecule of the disclosure includes two copies of a GITR-targeting fusion protein has the following structure: (GITR-BD)-Linker-(GITR-BD)-Linker-(GITR-BD)-Linker-Hinge-Fc, where the GITR-BD is an isolated polypeptide sequence that binds GITR. In some embodiments, the hexavalent GITR-targeting molecule of the disclosure includes two copies of a GITR-targeting fusion protein has the following structure: (GITR-BD)-Linker-(GITR-BD)-Linker-(GITR-BD)-Linker-Hinge-Fc, where the GITR-BD is an sdAb sequence that binds GITR. In some embodiments, the hexavalent GITR-targeting molecule of the disclosure includes two copies of a GITR-targeting fusion protein has the following structure: (GITR-BD)-Linker-(GITR-BD)-Linker-(GITR-BD)-Linker-Hinge-Fc, where the GITR-BD is a humanized or fully human sdAb sequence. In some embodiments, the tetravalent GITR-targeting molecule contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80. In some embodiments, the tetravalent GITR-targeting molecule contains at least one GITR-BD that comprises an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80. In some embodiments, the tetravalent GITR-targeting molecule contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62. In some embodiments, the tetravalent GITR-targeting molecule contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80. In some embodiments, the tetravalent GITR-targeting molecule comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 94-105.

The multivalent fusion proteins of the present disclosure are capable of enhanced clustering of TNFRSF members compared to non-cross-linked bivalent antibodies. The enhanced clustered of TNFRSF members mediated by the multivalent fusion proteins of the present disclosure induce enhanced TNFRSF-dependent signaling compared to non-cross-linked bivalent antibodies. In most embodiments, the multivalent fusion protein will incorporate more than two GITR-BDs, for example, three, four, five, or six. In these embodiments, the interaction of the non-TNFRSF antigen is capable of providing the additional crosslinking function and TNFRSF activation is achieved with only one or two TBDs.

In some embodiments, the multivalent fusion protein also includes one or more GITR-BDs and one or more additional binding domain(s) that bind to a target other than GITR. In some embodiments, the multivalent, multispecific fusion protein also includes one or more GITR-BDs and one or more additional binding domain(s) directed toward non-TNFRSF member antigen. In any of these embodiments, the multivalent, multispecific fusion protein can also include one or more additional binding domain(s) directed to a TNFRSF member, referred to herein as a TNFRSF-binding domain (TBD). In any of these embodiments, the interaction of the non-TNFRSF antigen is capable of providing the additional crosslinking function and TNFRSF activation is achieved with only one or two GITR-BDs or only one or two GITR-BDs and TBDs.

In some embodiments, the multivalent, multispecific fusion protein also includes one or more additional binding domain(s) directed to a TNFRSF member, referred to herein as a TNFRSF-binding domain (TBD). In these embodiments, the multivalent, multispecific fusion protein is binds at least two distinct antigens. In some embodiments, all of the TBDs of the multivalent, multispecific fusion protein recognize the same epitope on the given TNFRSF member. For example, the multivalent, multispecific fusion proteins of present disclosure may incorporate 2, 3, 4, 5, or 6 TBDs with identical specificity to a given TNFRSF member. In other embodiments, the multivalent, multispecific fusion protein incorporates TBDs that recognize distinct epitopes on the given TNFRSF member. For example, the multivalent, multispecific fusion proteins of present disclosure may incorporate 2, 3, 4, 5, or 6 TBDs with distinct recognition specificities toward various epitopes on GITR, CD40 or CD137. In these embodiments, the multivalent, multispecific fusion proteins of the present disclosure with contain multiple TBDs that target distinct regions of the particular TNFRSF member. In some embodiments, the TBDs may recognize different epitopes on the same TNFRSF member or recognize epitopes on distinct TNFRSF members. For example, the present disclosure provides multivalent, multispecific fusion proteins incorporating TBDs that bind GITR and OX40.

In other embodiments, the fusion proteins of the present disclosure is a multispecific fusion protein that binds GITR and a second TNFRSF member expressed on a non-tumor cell such as, by way of non-limiting example, OX40, CD27, HVEM, CD40, lymphotoxin beta receptor (LTBR), ectodysplasin A2 receptor (ED2R), ectodysplasin A receptor (EDAR), TweakR, BCMA, BAFFR, DR3, DR6 or CD137. In some embodiments, the multispecific fusion protein is also multivalent. In some embodiments, the multispecific fusion protein is bispecific. In these embodiments, the multispecific fusion proteins of the present disclosure modulate immune cells leading to enhanced tumor destruction. In other embodiments, the multispecific fusion proteins of the present disclosure have utility in treating inflammatory conditions. In these embodiments, the multispecific fusion proteins of the present disclosure modulate immune cells leading to dampening of the inflammatory insult. For example, specifically agonizing TNFR2 can enhance Treg proliferation leading to immune suppression.

In some embodiments, the multispecific fusion protein contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80. In some embodiments, the multispecific fusion protein contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62. In some embodiments, the multispecific fusion protein contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80.

In some embodiments, the multispecific fusion protein contains at least one GITR-BD that comprises an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80. In some embodiments, the multispecific fusion protein contains at least one GITR-BD that comprises an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62. In some embodiments, the multispecific fusion protein contains at least one GITR-BD that comprises an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80.

In some embodiments, the multispecific fusion protein contains at least one GITR-BD that comprises a complementarity determining region 1 (CDR1) comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 106, 109, 112, 117, 120, 125, 131, 138, 143, 148, and 149; a complementarity determining region 2 (CDR2) comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 107, 110, 113, 115, 118, 121, 123, 128, 130, 132, 134, 136, 137, 139, 141, 144, and 147; and a complementarity determining region 3 (CDR3) comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 108, 111, 114, 116, 119, 122, 124, 126, 127, 129, 133, 135, 140, 142, 145, 146, and 150.

In some embodiments, the multispecific fusion protein contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6. In some embodiments, the multispecific fusion protein contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6. In some embodiments, the multispecific fusion protein contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6.

In some embodiments, the multispecific fusion protein contains at least one GITR-BD that comprises an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6. In some embodiments, the multispecific fusion protein contains at least one GITR-BD that comprises an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6. In some embodiments, the multispecific fusion protein contains at least one GITR-BD that comprises an amino acid sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6.

In some embodiments, the multispecific fusion protein contains at least one GITR-BD that comprises a complementarity determining region 1 (CDR1) comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 106, 109, 112, 117, 120, 125, 131, 138, 143, 148, and 149; a complementarity determining region 2 (CDR2) comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 107, 110, 113, 115, 118, 121, 123, 128, 130, 132, 134, 136, 137, 139, 141, 144, and 147; and a complementarity determining region 3 (CDR3) comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 108, 111, 114, 116, 119, 122, 124, 126, 127, 129, 133, 135, 140, 142, 145, 146, and 150 and at least one immunoglobulin Fc region polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-6.

The multispecific fusion proteins of the present disclosure are capable of enhanced clustering of TNFRSF members compared to non-cross-linked bivalent antibodies. The enhanced clustered of TNFRSF members mediated by the multispecific fusion proteins of the present disclosure induce enhanced TNFRSF-dependent signaling compared to non-cross-linked bivalent antibodies. In most embodiments, the multispecific fusion protein will incorporate more than 2 TBDs, for example, three, four, five, or six. In some embodiments, the multispecific fusion protein will incorporate TBDs and a binding domain directed toward non-TNFRSF member antigen. In these embodiments, the interaction of the non-TNFRSF antigen is capable of providing the additional crosslinking function and TNFRSF activation is achieved with only one or two TBDs. In these embodiments, the multispecific fusion protein is multispecific, binding two distinct antigens.

In some embodiments, TBDs of the present disclosure are derived from antibodies or antibody fragments including scFv, Fabs, single domain antibodies (sdAb), V_(NAR), or VHHs. In some embodiments, the TBDs are human or humanized sdAb. The sdAb fragments can be derived from VHH, V_(NAR), engineered VH or VK domains. VHHs can be generated from camelid heavy chain only antibodies. V_(NAR)s can be generated from cartilaginous fish heavy chain only antibodies. Various methods have been implemented to generate monomeric sdAbs from conventionally heterodimeric VH and VK domains, including interface engineering and selection of specific germline families. In other embodiments, the TDBs are derived from non-antibody scaffold proteins for example but not limited to designed ankyrin repeat proteins (darpins), avimers, anticalin/lipocalins, centyrins and fynomers.

Generally the multispecific fusion proteins of the present disclosure consist of at least two or more TBDs operably linked via a linker polypeptide. The utilization of sdAb fragments as the specific TBD within the multispecific fusion the present disclosure has the benefit of avoiding the heavy chain:light chain mis-pairing problem common to many bi/multispecific antibody approaches. In addition, the multispecific fusion proteins of the present disclosure avoid the use of long linkers necessitated by many bispecific antibodies.

In some embodiments, all of the TBDs of the multispecific fusion protein recognize the same epitope on the given TNFRSF member. For example, the multispecific fusion proteins of present disclosure may incorporate 2, 3, 4, 5, or 6 TBDs with identical specificity to GITR. In other embodiments, the multispecific fusion protein incorporates TBDs that recognize distinct epitopes on the given TNFRSF member. For example, the multispecific fusion proteins of present disclosure may incorporate 2, 3, 4, 5, or 6 TBDs with distinct recognition specificities toward various epitopes on GITR, CD40 or CD137. In these embodiments, the multispecific fusion proteins of the present disclosure with contain multiple TBDs that target distinct regions of the particular TNFRSF member. In some embodiments, the TBDs may recognize different epitopes on the same TNFRSF member or recognize epitopes on distinct TNFRSF members. For example, the present disclosure provides multispecific fusion proteins incorporating TBDs that bind GITR and OX40.

In some embodiments, the fusion protein of the present disclosure, e.g. multivalent and/or multispecific fusion proteins, is composed of a single polypeptide. In other embodiments, the fusion protein of the present disclosure is composed of more than one polypeptide. For example, a heterodimerization domain is incorporated into the fusion protein such that the construct is an asymmetric fusion protein. For example, if an immunoglobulin Fc region is incorporated into the fusion protein, the CH3 domain can be used as homodimerization domain, or the CH3 dimer interface region can be mutated so as to enable heterodimerization.

In some embodiments, the fusion protein contains the TBDs and/or GITR-BDs at opposite ends of the fusion protein. For example, in some embodiments, the TBDs and/or GITR-BDs are located on both the amino-terminal (N-terminal) portion of the fusion protein and the carboxy-terminal (C-terminal) portion of the fusion protein. In other embodiments, all the TBDs and/or GITR-BDs reside on the same end of the fusion protein. For example, TBDs and/or GITR-BDs reside on either the amino or carboxyl terminal portions of the fusion protein.

In some embodiments, the fusion protein contains an immunoglobulin Fc region. In some embodiments, the immunoglobulin Fc region is an IgG isotype selected from the group consisting of IgG1 isotype, IgG2 isotype, IgG3 isotype, and IgG4 subclass.

In some embodiments, the immunoglobulin Fc region or immunologically active fragment thereof is an IgG isotype. For example, the immunoglobulin Fc region of the fusion protein is of human IgG1 isotype, having an amino acid sequence:

(SEQ ID NO: 1)

HQDWLNGKEY KCKVSNKALP APIEKTISKA KGQPREPQVY TLPPSRDELT KNQVSLTCLV KGFYPSDIAV EWESNGQPEN NYKTTPPVLD SDGSFFLYSK LTVDKSRWQQ GNVFSCSVMH EALHNHYTQK SLSLSPGK

In some embodiments, the immunoglobulin Fc region or immunologically active fragment thereof comprises a human IgG1 polypeptide sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to the amino acid sequence of SEQ ID NO: 1.

In some embodiments, the human IgG1 Fc region is modified at amino acid Asn297 (Boxed, Kabat Numbering) to prevent to glycosylation of the fusion protein, e.g., Asn297Ala (N297A) or Asn297Asp (N297D). In some embodiments, the Fc region of the fusion protein is modified at amino acid Leu235 (Boxed, Kabat Numbering) to alter Fc receptor interactions, e.g., Leu235Glu (L235E) or Leu235Ala (L235A). In some embodiments, the Fc region of the fusion protein is modified at amino acid Leu234 (Boxed, Kabat Numbering) to alter Fc receptor interactions, e.g., Leu234Ala (L234A). In some embodiments, the Fc region of the fusion protein is modified at amino acid Leu234 (Boxed, Kabat Numbering) to alter Fc receptor interactions, e.g., Leu235Glu (L235E). In some embodiments, the Fc region of the fusion protein is altered at both amino acids 234 and 235, e.g., Leu234Ala and Leu235Ala (L234A/L235A) or Leu234Val and Leu235Ala (L234V/L235A). In some embodiments, the Fc region of the fusion protein is altered at Gly235 to reduce Fc receptor binding. For example, wherein Gly235 is deleted from the fusion protein. In some embodiments, the human IgG1 Fc region is modified at amino acid Gly236 to enhance the interaction with CD32A, e.g., Gly236Ala (G236A). In some embodiments, the human IgG1 Fc region is lacks Lys447 (EU index of Kabat et al 1991 Sequences of Proteins of Immunological Interest).

In some embodiments, the Fc region of the fusion protein is altered at one or more of the following positions to reduce Fc receptor binding: Leu 234 (L234), Leu235 (L235), Asp265 (D265), Asp270 (D270), Ser298 (S298), Asn297 (N297), Asn325 (N325) orAla327 (A327). For example, Leu 234Ala (L234A), Leu235Ala (L235A), Asp265Asn (D265N), Asp270Asn (D270N), Ser298Asn (S298N), Asn297Ala (N297A), Asn325Glu (N325E) orAla327Ser (A327S). In preferred embodiments, modifications within the Fc region reduce binding to Fc-receptor-gamma receptors while have minimal impact on binding to the neonatal Fc receptor (FcRn).

In some embodiments, the Fc region of the fusion protein is lacking an amino acid at one or more of the following positions to reduce Fc receptor binding: Glu233 (E233), Leu234 (L234), or Leu235 (L235). In these embodiments, Fc deletion of these three amino acids reduces the complement protein C1q binding. These modified Fc region polypeptides are referred to herein as “Fc deletion” polypeptides.

(SEQ ID NO: 2) PAPGGPSVFL YPPKTKDTLM ISRTPEVTCV VVDVSHEDPE VKFNQYVDGV EVHNAKTKPR EEQYNSTYRV VSVLTVLHQD WLNGKEYKCK VSNKALPAPI EKTISKAKGQ PREPQVYTLP PSRDELTKNQ VSLTCLVKGF YPSDIAVEWE SNGQPENNYK TTPPVLDSDG SFFLYSKLTV DKSRWQQGNV FSCSVMHEAL HNHYTQKSLS LSPGX

In some embodiments, the immunoglobulin Fc region or immunologically active fragment thereof comprises a human IgG1 polypeptide sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to the amino acid sequence of SEQ ID NO: 2.

In some embodiments, the immunoglobulin Fc region or immunologically active fragment of the fusion protein is of human IgG2 isotype, having an amino acid sequence:

(SEQ ID NO: 3) PAPPVAGPSV FLFPPKPKDT LMISRTPEVT CVVVDVSHED

QDWLNGKEYK CKVSNKGLPA PIEKTISKTK GQPREPQVYT LPPSREEMTK NQVSLTCLVK GFYPSDISVE WESNGQPENN YKTTPPMLDS DGSFFLYSKL TVDKSRWQQG NVFSCSVMHE ALHNHYTQKS LSLSPGK

In some embodiments, the fusion or immunologically active fragment thereof comprises a human IgG2 polypeptide sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to the amino acid sequence of SEQ ID NO: 3.

In some embodiments, the human IgG2 Fc region is modified at amino acid Asn297 (Boxed, to prevent to glycosylation of the antibody, e.g., Asn297Ala (N297A) or Asn297Asp (N297D). In some embodiments, the human IgG2 Fc region is lacks Lys447 (EU index of Kabat et al 1991 Sequences of Proteins of Immunological Interest).

In some embodiments, the immunoglobulin Fc region or immunologically active fragment of the fusion protein is of human IgG3 isotype, having an amino acid sequence:

(SEQ ID NO: 4) PAPELLGGPS VFLFPPKPKD TLMISRTPEV TCVVVDVSHE

HQDWLNGKEY KCKVSNKALP APIEKTISKT KGQPREPQVY TLPPSREEMT KNQVSLTCLV KGFYPSDIAV EWESSGQPEN NYNTTPPMLD SDGSFFLYSK LTVDKSRWQQ GNIFSCSVMH

In some embodiments, the antibody or immunologically active fragment thereof comprises a human IgG3 polypeptide sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to the amino acid sequence of SEQ ID NO: 4.

In some embodiments, the human IgG3 Fc region is modified at amino acid Asn297 (Boxed, Kabat Numbering) to prevent to glycosylation of the antibody, e.g., Asn297Ala (N297A) or Asn297Asp (N297D). In some embodiments, the human IgG3 Fc region is modified at amino acid 435 to extend the half-life, e.g., Arg435His (R435H). In some embodiments, the human IgG3 Fc region is lacks Lys447 (EU index of Kabat et al 1991 Sequences of Proteins of Immunological Interest).

In some embodiments, the immunoglobulin Fc region or immunologically active fragment of the fusion protein is of human IgG4 isotype, having an amino acid sequence:

(SEQ ID NO: 5)

HQDWLNGKEY KCKVSNKGLP SSIEKTISKA KGQPREPQVY TLPPSQEEMT KNQVSLTCLV KGFYPSDIAV EWESNGQPEN NYKTTPPVLD SDGSFFLYSR LTVDKSRWQE GNVFSCSVMH EALHNHYTQK SLSLSLGK

In some embodiments, the antibody or immunologically active fragment thereof comprises a human IgG4 polypeptide sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to the amino acid sequence of SEQ ID NO: 5.

In some embodiments, the immunoglobulin Fc region or immunologically active fragment of the fusion protein is of human IgG4 isotype, having an amino acid sequence:

(SEQ ID NO: 6) PAPELLGGPS VFLFPPKPKD TLMISRTPEV TCVVVDVSQE

HQDWLNGKEY KCKVSNKGLP SSIEKTISKA KGQPREPQVY TLPPSQEEMT KNQVSLTCLV KGFYPSDIAV EWESNGQPEN NYKTTPPVLD SDGSFFLYSR LTVDKSRWQE GNVFSCSVMH EALHNHYTQK SLSLSLGK

In some embodiments, the antibody or immunologically active fragment thereof comprises a human IgG4 polypeptide sequence that is at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to the amino acid sequence of SEQ ID NO: 6.

In other embodiments, the human IgG4 Fc region is modified at amino acid 235 to alter Fc receptor interactions, e.g., Leu235Glu (L235E). In some embodiments, the human IgG4 Fc region is modified at amino acid Asn297 (Kabat Numbering) to prevent to glycosylation of the antibody, e.g., Asn297Ala (N297A) or Asn297Asp (N297D). In some embodiments, the human IgG4 Fc region is lacks Lys447 (EU index of Kabat et al 1991 Sequences of Proteins of Immunological Interest).

In some embodiments, the human IgG Fc region is modified to enhance FcRn binding. Examples of Fc mutations that enhance binding to FcRn are Met252Tyr, Ser254Thr, Thr256Glu (M252Y, S254T, T256E, respectively) (Kabat numbering, Dall'Acqua et al 2006, J. Biol Chem Vol. 281(33) 23514-23524), Met428Leu and Asn434Ser (M428L, N434S) (Zalevsky et al 2010 Nature Biotech, Vol. 28(2) 157-159), or Met252Ile, Thr256Asp, Met428Leu (M252I, T256D, M428L, respectively), (EU index of Kabat et al 1991 Sequences of Proteins of Immunological Interest).

In some embodiments where the fusion protein of the disclosure includes an Fc polypeptide, the Fc polypeptide is mutated or modified. In these embodiments, the mutated or modified Fc polypeptide includes the following mutations: Met252Tyr and Met428Leu (M252Y, M428L) using the Kabat numbering system.

In some embodiments, the human IgG Fc region is modified to alter antibody-dependent cellular cytotoxicity (ADCC) and/or complement-dependent cytotoxicity (CDC), e.g., the amino acid modifications described in Natsume et al., 2008 Cancer Res, 68(10): 3863-72; Idusogie et al., 2001 J Immunol, 166(4): 2571-5; Moore et al., 2010 mAbs, 2(2): 181-189; Lazar et al., 2006 PNAS, 103(11): 4005-4010, Shields et al., 2001 JBC, 276(9): 6591-6604; Stavenhagen et al., 2007 Cancer Res, 67(18): 8882-8890; Stavenhagen et al., 2008 Advan. Enzyme Regul., 48: 152-164; Alegre et al, 1992 J Immunol, 148: 3461-3468; Reviewed in Kaneko and Niwa, 2011 Biodrugs, 25(1):1-11. Examples of mutations that enhance ADCC include modification at Ser239 and Ile332, for example Ser239Asp and Ile332Glu (S239D, I332E). Examples of mutations that enhance CDC include modifications at Lys326 and Glu333. In some embodiments, the Fc region is modified at one or both of these positions, for example Lys326Ala and/or Glu333Ala (K326A and E333A) using the Kabat numbering system.

In some embodiments, the human IgG Fc region is modified to induce heterodimerization. For example, having an amino acid modification within the CH3 domain at Thr366, which when replaced with a more bulky amino acid, e.g., Try (T366W), is able to preferentially pair with a second CH3 domain having amino acid modifications to less bulky amino acids at positions Thr366, Leu368, and Tyr407, e.g., Ser, Ala and Val, respectively (T366S/L368A/Y407V). Heterodimerization via CH3 modifications can be further stabilized by the introduction of a disulfide bond, for example by changing Ser354 to Cys (S354C) and Y349 to Cys (Y349C) on opposite CH3 domains (Reviewed in Carter, 2001 Journal of Immunological Methods, 248: 7-15).

In some embodiments, the human IgG Fc region is modified to prevent dimerization. In these embodiments, the fusion proteins of the present disclosure are monomeric. For example modification at residue Thr366 to a charged residue, e.g. Thr366Lys, Thr366Arg, Thr366Asp, or Thr366Glu (T366K, T366R, T366D, or T366E, respectively), prevents CH3-CH3 dimerization.

In some embodiments, the Fc region of the fusion protein is altered at one or more of the following positions to reduce Fc receptor binding: Leu 234 (L234), Leu235 (L235), Asp265 (D265), Asp270 (D270), Ser298 (S298), Asn297 (N297), Asn325 (N325) orAla327 (A327). For example, Leu 234Ala (L234A), Leu235Ala (L235A), Asp265Asn (D265N), Asp270Asn (D270N), Ser298Asn (S298N), Asn297Ala (N297A), Asn325Glu (N325E) orAla327Ser (A327S). In preferred embodiments, modifications within the Fc region reduce binding to Fc-receptor-gamma receptors while have minimal impact on binding to the neonatal Fc receptor (FcRn).

In some embodiments, the fusion protein contains a polypeptide derived from an immunoglobulin hinge region. The hinge region can be selected from any of the human IgG subclasses. For example, the fusion protein may contain a modified IgG1 hinge having the sequence of EPKSSDKTHTCPPC (SEQ ID NO: 7), where in the Cys220 that forms a disulfide with the C-terminal cysteine of the light chain is mutated to serine, e.g., Cys220Ser (C220S). In other embodiments, the fusion protein contains a truncated hinge having a sequence DKTHTCPPC (SEQ ID NO: 8).

In some embodiments, the fusion protein has a modified hinge from IgG4, which is modified to prevent or reduce strand exchange, e.g., Ser228Pro (S228P), having the sequence ESKYGPPCPPC (SEQ ID NO: 9). In some embodiments, the fusion protein contains linker polypeptides. In other embodiments, the fusion protein contains linker and hinge polypeptides.

In some embodiments, the fusion proteins of the present disclosure lack or have reduced Fucose attached to the N-linked glycan-chain at N297. There are numerous ways to prevent fucosylation, including but not limited to production in a FUT8 deficient cell line; addition inhibitors to the mammalian cell culture media, for example Castanospermine; and metabolic engineering of the production cell line.

In some embodiments, the TBD is engineered to eliminate recognition by pre-existing antibodies found in humans. In some embodiments, single domain antibodies of the present disclosure are modified by mutation of position Leu11, for example Leu11Glu (L11E) or Leu11Lys (L11K). In other embodiments, single domain antibodies of the present disclosure are modified by changes in carboxy-terminal region, for example the terminal sequence consists of GQGTLVTVKPGG (SEQ ID NO: 10) or GQGTLVTVEPGG (SEQ ID NO: 11) or modification thereof. In some embodiments, the single domain antibodies of the present disclosure are modified by mutation of position 11 and by changes in carboxy-terminal region.

In some embodiments, the TBDs and/or GITR-BDs of the fusion proteins of the present disclosure are operably linked via amino acid linkers. In some embodiments, these linkers are composed predominately of the amino acids Glycine and Serine, denoted as GS-linkers herein. The GS-linkers of the fusion proteins of the present disclosure can be of various lengths, for example, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20 amino acids in length.

In some embodiments, the GS-linker comprises an amino acid sequence selected from the group consisting of GGSGGS, i.e., (GGS)₂ (SEQ ID NO: 12); GGSGGSGGS, i.e., (GGS)₃ (SEQ ID NO: 13); GGSGGSGGSGGS, i.e., (GGS)₄ (SEQ ID NO: 14); and GGSGGSGGSGGSGGS, i.e., (GGS)₅ (SEQ ID NO: 15).

In some embodiments, the linker is a flexible linker comprising Glycine residues, such as, by way of non-limiting example, GG, GGG, GGGG (SEQ ID NO: 16), GGGGG (SEQ ID NO: 17), and GGGGGG (SEQ ID NO: 18).

In some embodiments, the GITR-targeting fusion protein includes a combination of a GS-linker and a Glycine linker.

BRIEF DESCRIPTION OF FIGURES

FIG. 1 is schematic representation of exemplary multivalent fusion proteins of the present disclosure.

FIGS. 2A, 2B, and 2C are a series of graphs demonstrating the binding of GITR-targeting fusion proteins to GITR expressed on CHO cells as assessed by flow cytometry. The GITR antibody, TRX-518, was used as a control for these studies.

FIGS. 3A, 3B, and 3C are a series of graphs demonstrating the ability of GITR-targeting fusion proteins to block the interaction between GITRL and GITR. Herein, a flow cytometry assay using GITR expressing CHO cells and recombinant GITRL was used to assess blocking capacity. The GITR antibody, TRX-518, was used as a control for these studies.

FIGS. 4A, 4B, 4C, 4D, 4E, and 4F are a series of graphs depicting the binding of the GITR-targeting molecules of the disclosure referred to as hzC06v1.1, hzC06v1.2, hzC06v1.3, hzC06v1.4, hzC06v2.1, hzC06v2.2, hzC06v2.3, hzC06v2.4, hzC06v3, hzC06v3.1, hzC06v3.2, hzC06v3.3, hzC06v3.4, hzC06v3.5, hzC06v3.6, hzC06v3.7, hzC06v3.8, hzC06v3.9, hzC06v3.10, hzC06v3.11, and hzC06v3.12 for human GITR and cynomolgus GITR (“cyno GITR”) expressed on the surface of CHO cells, as measured by flow cytometry.

FIGS. 5A, 5B, 5C, 5D, 5E, 5F, and 5G are a series of graphs depicting the binding of the GITR-targeting molecules of the disclosure referred to as hzC04v4.1, hzC04v4.1.2, hzC04v4.2, hzC04v4.2.2, hzC04v5, hzC04v1.2.1, hzC04v5.1, hzC04v5.2, hzC04v5.3, hzC04v5.4, hzC04v5.5, hzC04v5.6, hzC04v5.7, hzC04v5.8, hzC04v5.9, hzC04v5.10, hzC04v5.11, and hzC04v5.12 for human GITR and cynomolgus GITR (“cyno GITR”) expressed on the surface of CHO cells, as measured by flow cytometry.

FIG. 6 is a schematic representation of tetravalent anti-GITR molecules of the disclosure, which are constructed with two tandem copies of a single-domain variable region (sdAb) fused to a human IgG1 Fc domain. Surrogate molecules are constructed with Fc domains derived from mouse IgG2a.

FIG. 7 is a graph depicting the binding an anti-GITR molecule of the disclosure, referred to herein as tetravalent hzC06-hIgG1, to primary human T cells. Tetravalent hzC06-hIgG1 is constructed with two copies of the GITR-binding molecule of SEQ ID NO: 93, which, in turn, is constructed with two tandem copies of a single-domain variable region (sdAb) of SEQ ID NO: 59 fused to a human IgG1 Fc domain of SEQ ID NO: 1.

FIGS. 8A and 8B are a series of graphs depicting the ability of tetravalent GITR-targeting molecules of the disclosure to activate NF-kB signaling in reporter cell lines expressing GITR.

FIGS. 9A, 9B, and 9C are a series of graphs depicting that treatment with a tetravalent GITR-targeting molecule of the disclosure significantly reduced CT26 tumor growth irrespective of day of administration.

FIG. 10 is a series of graphs depicting the dose-dependent suppression of CT26 tumor growth by a tetravalent GITR-targeting molecule of the disclosure.

FIGS. 11A and 11B are a series of graphs depicting the dose-dependent suppression of MC38 tumor growth by a tetravalent GITR-targeting molecule of the disclosure.

FIGS. 12A, 12B, and 12C are a series of graphs depicting the impact of Fc function on inhibition of CT26 tumor growth.

FIGS. 13A, 13B, and 13C are a series of graphs depicting that treatment with a tetravalent GITR-targeting molecule had subsequence resistance to re-challenge with CT26 tumors.

FIGS. 14A, 14B, and 14C are a series of graphs depicting that treatment with a tetravalent GITR-targeting molecule of the disclosure significantly reduced T_(reg) frequency and altered the ratio of T_(reg) to T_(effector) cells within the tumor microenvironment.

FIGS. 15A and 15B are a series of graphs depicting that treatment with a tetravalent GITR-targeting molecule of the disclosure significantly induced CD8 T cell activation and proliferation.

DETAILED DESCRIPTION

The disclosure provides molecules that specifically engage glucocorticoid-induced TNFR-related protein (GITR), a member of the TNF receptor superfamily (TNFRSF). More specifically this disclosure relates to multivalent molecules that bind at least GITR. These multivalent TNFRSF binding fusion proteins comprise two or more TNFRSF binding domains (TBDs), where at least one TBD binds GITR, referred to herein as a “GITR-binding domain” (GITR-BD).

GITR is a member of the TNFRSF and is constitutively expressed on CD4+/CD25+/Foxop3+ regulatory T-cells (Treg) in a tumor and upregulated on other T-cell populations following activation. It is hypothesized to have and dominant role in Treg-mediated immunological self-tolerance. GITR agonists dampen the suppressive activities of Tregs and in mouse models have been shown to enhance effector T-cell killing of tumors. Therefore a functional GITR agonist has great potential tumor immunotherapy.

In some embodiments, the fusion proteins of the present disclosure incorporate at least one GITR-BD. In some embodiments, the fusion protein is a multivalent fusion protein. In some embodiments, the fusion protein is a multispecific fusion protein that binds GITR and a second antigen, such as, for example, any other TNFRSF member. In some embodiments, the fusion protein is a multispecific and multivalent fusion protein.

In some embodiments, the GITR-BD binds human and cynomolgus monkey GITR. In some embodiments, the GITR-BD blocks, inhibits or otherwise modulates the interaction of GITR and its ligand GITR-Ligand (GITR-L). In other embodiments, the GITR-BD does not block, inhibit or otherwise modulate the interaction of GITR and GITR-L. In some embodiments, the fusion protein of the present disclosure incorporates multiple copies of the same GITR-BD. In some embodiments, the fusion protein of the present disclosure incorporates multiple GITR-BDs that recognize the same epitope on GITR. In some embodiments, the fusion protein of the present disclosure incorporates multiple GITR-BDs that recognize distinct epitopes on GITR. In some embodiments, the fusion protein of the present disclosure incorporates multiple GITR-BDs, wherein some GITR-BDs block the GITR-GITR-L interaction and other do not block the GITR-GITR-L interaction. In preferred embodiments, GITR-targeting fusion proteins of the present disclosure induce direct cell death of tumor cells.

In some embodiments, the GITR-targeting molecule includes at least one copy of a single-domain antibody (sdAb) sequence that specifically binds GITR. In some embodiments, the GITR-targeting molecules include two or more copies of an sdAb that specifically binds GITR, for example, three or more, four or more, five or more, or six or more copies of an sdAb that specifically binds GITR.

A single-domain antibody (sdAb) is an antibody fragment consisting of a single monomeric variable antibody domain that is able to bind selectively to a specific antigen. With a molecular weight of only 12-15 kDa, single-domain antibodies are much smaller than common antibodies (150-160 kDa) which are composed of two heavy protein chains and two light chains, and even smaller than Fab fragments (˜50 kDa, one light chain and half a heavy chain) and single-chain variable fragments (˜25 kDa, two variable domains, one from a light and one from a heavy chain).

Single domain antibodies are antibodies whose complementary determining regions are part of a single domain polypeptide. Examples include, but are not limited to, heavy chain antibodies, antibodies naturally devoid of light chains, single domain antibodies derived from conventional 4-chain antibodies, engineered antibodies and single domain scaffolds other than those derived from antibodies. Single domain antibodies may be derived from any species including, but not limited to mouse, human, camel, llama, goat, rabbit, and/or bovine. In some embodiments, a single domain antibody as used herein is a naturally occurring single domain antibody known as heavy chain antibody devoid of light chains. For clarity reasons, this variable domain derived from a heavy chain antibody naturally devoid of light chain is known herein as a VHH to distinguish it from the conventional VH of four chain immunoglobulins. Such a VHH molecule can be derived from antibodies raised in Camelidae species, for example in camel, llama, dromedary, alpaca and guanaco. Other species besides Camelidae may produce heavy chain antibodies naturally devoid of light chain; such VHHs are within the scope of the disclosure.

GITR VHH (llama-derived) and humanized sequences are shown below, and the CDR sequences are shown in the sequences presented below. In some embodiments, the GITR-binding sdAb is fused to an IgG Fc region and in these embodiments, the fusion protein is bivalent having two GITR-binding domains per molecule. In some embodiments, two GITR-binding sdAbs (2×) are fused to an IgG Fc region and in these embodiments, the fusion protein is tetravalent having four GITR-binding domains per molecule. In some embodiments, three GITR-binding sdAbs (3×) are fused to an IgG Fc region and in these embodiments, the fusion protein is hexavalent having six GITR-binding domains per molecule.

Exemplary GITR-Binding sdAbs

B09  (SEQ ID NO: 19) QVQLQESGGXLVQSGGSLRLSCAASGSVFSIDAMGWYRLAPGKQRELVAVMSSGSPKYADSVK  GRFTISRGSARGTVYLQMDSLKPEDTAVYYCYADVATGWGRDASAYWGQGTQVTVSS CDR1:  (SEQ ID NO: 106) GSVFSIDAM  CDR2:  (SEQ ID NO: 107) VMSSGSPK  CDR3:  (SEQ ID NO: 108) YADVATGWGRDASAYW  H09  (SEQ ID NO: 20) QVQLQQSGGGLVRAGGSLRLSCVAAGSTFSVNSMAWYRQAPGKERELVAAFTGGSTMNYASSV  KGRFTISRGNAAHTVLLQMTNLKPEDTAVYYCNAEVNEGWNADYHDYWGQGTQVTVSS CDR1:  (SEQ ID NO: 109) AGSTFSVNSM  CDR2:  (SEQ ID NO: 110) FTGGSTMN  CDR3:  (SEQ ID NO: 111) NAEVNEGWNADYHDYW F05  (SEQ ID NO: 21) QVQLVQSGGGLVQAGGSLRLSCTASGSIFSINHMAWYRQAPGKQREMVAHITGGASTKYADSV KGRFTISRDSALNTVSLRMNSLKPEDTAVYYCNAEVNEGWNADYYDVWGQGTQVTVSS CDR1:  (SEQ ID NO: 112) SGSIFSINHM CDR2:  (SEQ ID NO: 113) HITGGASTK  CDR3:  (SEQ ID NO: 114) NAEVNEGWNADYYDVW  C06  (SEQ ID NO: 22) QVQLQESGGGLVQAGGSLRLSCAASGSVFSIDAMGWYRLAPGQQRELVAVLNGISSAKYADSV KGRFTISGDSAKNAVYLQMDGLKPEDTAVYYCYADVSTGWGRDAHGYWGQGTQVTVSS CDR1:  (SEQ ID NO: 106) GSVFSIDAM  CDR2:  (SEQ ID NO: 115) VLNGISSAK  CDR3:  (SEQ ID NO: 116) YADVSTGWGRDAHGYW  2A1  (SEQ ID NO: 23) EVQLVQSGGGLVQPGGSLRLSCAASGNIFSIDAMGWYRQAPGRQRELVAQIPGGPTDSVKGRF  TVSGNSAKNTGYLQMNTLKPEDTAVYYCNIVASTSWGSPSKVYWGQGTQATVSS  CDR1:  (SEQ ID NO: 117) SGNIFSIDAM  CDR2:  (SEQ ID NO: 118) QIPGG  CDR3:  (SEQ ID NO: 119) NIVASTSWGSPSKVYW  E2  (SEQ ID NO: 24) QVQLQESGGGLVQPGGSLRLSCAASGSVFSIDSMSWFRQAPGNERELVALITGGRTTTYADSV  KGRFTISRASAPNTVYLQMNSLKPEDTAVYYCNAVVSTGWGRNADDYWGQGTQVTVS  CDR1:  (SEQ ID NO: 120) SGSVFSIDSM  CDR2:  (SEQ ID NO: 121) LITGGRTTT  CDR3:  (SEQ ID NO: 122) NAVVSTGWGRNADDYW  B12  (SEQ ID NO: 25) QVQLQQSGGGLVQAGGSLRLSCAASGSIFSIDAMGWYRLAPGKQRELVAVIDGVSPNYADSVK  GRFTISSDIAKNTVYLQMHSPKPEDTAVYCNADVSTGWGRPADHYWGQGTQVTVS  CDR1:  (SEQ ID NO: 149) SGSIFSIDAM  CDR2:  (SEQ ID NO: 123) VIDGVSPN  CDR3:  (SEQ ID NO: 150) NADVSTGWGRPADHYW  B2  (SEQ ID NO: 26) QVQLQESGGGLVQPGGSLRLSCAASGSVFSIDSMSWFRQAPGNERELVALITGGHTTTYGDSV  KGRFTISRASAPNTVHLQMNSLQPFDTAVYYCNAAVSTGWGRNADDYWGQGTQVTVS  CDR1:  (SEQ ID NO: 120) SGSVFSIDSM  CDR2:  (SEQ ID NO: 123) LITGGHTTT  CDR3:  (SEQ ID NO: 124) NAAVSTGWGRNADDYW  F2  (SEQ ID NO: 27) QLVQSGGGLVQPGESLRLSCAASGSVFSIDSVSWFRQGPGNERELVALITGGRTTTYADSVKG  RFTISRANAPNTVHLRMNSLKPEDTAVYYCNAAVSTGWGRNADDYWGQGTQVTVS CDR1:  (SEQ ID NO: 125) SGSVFSIDSV  CDR2:  (SEQ ID NO: 121) LITGGRITT  CDR3:  (SEQ ID NO: 124) NAAVSTGWGRNADDYW  B3  (SEQ ID NO: 28) QVQLVQSGGGLVQPGGSLRLICAASGSVFSIDSMSWFRQRPGNERELVALITGGRTTTYSDSV KGRFTISRASALNTVHLQMNSLKPEDTAVYYCNAALSTGWGRDASAYWGQGTQVTVS CDR1:  (SEQ ID NO: 120) SGSVFSIDSM  CDR2:  (SEQ ID NO: 121) LITGGRTTT  CDR3:  (SEQ ID NO: 126) NAALSTGWGRDASAYW  E3  (SEQ ID NO: 29) QVQLQESGGGLVQAGGSLRLSCTASGSIFSINHMAWYRQAPGKQREMVAHITGGASTKYADSV  KGRFTISRDSALNTVSLRMNSLKPEDTAVYYCNAEVNEGWNADYYDVWGQGTQVTVS  CDR1:  (SEQ ID NO: 112) SGSIFSINHM  CDR2:  (SEQ ID NO: 113) HITGGASTK  CDR3:  (SEQ ID NO: 127) AEVNEGWNADYYDVW  B4  (SEQ ID NO: 30) QLQLQESGGGTVQAGGSLRLSCAASRSIASINVMGWYRQAPGNQHELVAAITSGGSPNYAGSV RGRFIISRDNAKNIVYLQMNDLKPEDTAVYYCAGELRDDSNGYLHYWGQGTQVTVS  CDR1:  (SEQ ID NO: 148) SRSIASINVM  CDR2:  (SEQ ID NO: 128) ITSGGSPN  CDR3:  (SEQ ID NO: 129) AGELRDDSNGYLHYW  B7  (SEQ ID NO: 31) QVQLQESGGGLVQPGGSLRLSCAASGSVFSIDSMSWFRQTPGNERELVAHITGGRTTTYADSV KGRFTISRASAPNTVHLQMNNLKPEDTAVYYCNAAVSTGWGRNADDYWGQGTQVTVS  CDR1:  (SEQ ID NO: 120) SGSVFSIDSM  CDR2:  (SEQ ID NO: 130) HITGGRTTT  CDR3:  (SEQ ID NO: 124) NAAVSTGWGRNADDYW  C7  (SEQ ID NO: 32) QVQLQESGGGLVQAGGSLRLSCTASGSIFSIDDMGWYRLAPGKQRELVAVHSGSSTNYGDSVK  GRFTISGDSAKNTVYLQMHRLEPEDTAVYYCYAAISSGWGRDAEDYWGQGTQVTVS  CDR1:  (SEQ ID NO: 131) SGSIFSIDDM  CDR2:  (SEQ ID NO: 132) VHSGSSTN  CDR3:  (SEQ ID NO: 133) YAAISSGWGRDAEDYW  C4  (SEQ ID NO: 33) QVQLVQSGGGLVQPGESLRLSCAASGSVFSIDSMSWFRQGPGNERELVALTIGGRTTTYADSV  KGRFTISRANAPNTVHLQMNSLKPEDTAVYYCNAAVSTGWGRSADDYWGQGTQVTVS  CDR1:  (SEQ ID NO: 120) SGSVFSIDSM  CDR2:  (SEQ ID NO: 134) ITGGRTTT  CDR3:  (SEQ ID NO: 135) NAAVSTGWGRSADDYW  B5  (SEQ ID NO: 34) QVQLVQSGGGLVQPGESLRLSCAASGSVFSIDSMSWFRQGPGNERELVALITGGRTTTYADSV  KGRFTISRANAPNTVHLQMNSLEPEDTAVYYCNAAVSTGWGRNADDYWGQGTQVTVS  CDR1:  (SEQ ID NO: 120) SGSVFSIDSM  CDR2:  (SEQ ID NO: 121) LITGGRTTT  CDR3:  (SEQ ID NO: 124) NAAVSTGWGRNADDYW  H11  (SEQ ID NO: 35) QVQLVQSGGGLVQPGGSLRLSCAASGSVFSIDSMSWFKQAPGNERELVALITCGRTTTYADSV  KGRFTISRASAPNTVHLQMNSLKPEDTAVYYCNAVVSTGWGRNADDYWGQGTQVTVS  CDR1:  (SEQ ID NO: 120) SGSVFSIDSM  CDR2:  (SEQ ID NO: 121) LITGGRTTT  CDR3:  (SEQ ID NO: 122) NAVVSTGWGRNADDYW  H11v420  (SEQ ID NO: 36) EVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGLELVSAITGGRTTYYAESV  KGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNADDYWGQGTLVTVKP  CDR1:  (SEQ ID NO: 106) GSVFSIDAM  CDR2:  (SEQ ID NO: 137) ITGGRTTY  CDR3:  (SEQ ID NO: 122) NAVVSTGWGRNADDYW  H11v420.1  (SEQ ID NO: 37) EVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGLELVCAITGGRTTYYAESV  KGRFTCSRDNAKNTLYLMSSLRAEDTAVYYCNAVVSTGWGRNADDYWGQGTLVTVKP  CDR1:  (SEQ ID NO: 106) GSVFSIDAM  CDR2:  (SEQ ID NO: 137) AITGGRTTY  CDR3:  (SEQ ID NO: 122) NAVVSTGWGRNADDYW  H11v401  (SEQ ID NO: 38) EVQLLESGGGEVQPGGSLRLSCAASGSVFSIDSMSWFRQAPGKGLELVSLITGGRTTYAESV  KGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCNNVVSTGWGRNADDYWGQGTLVTVKP  CDR1:  (SEQ ID NO: 120) SGSVFSIDSM  CDR2:  (SEQ ID NO: 137) LITGGRTTY  CDR3: (SEQ ID NO: 122) NAVVSTGWGRNADDYW  H11v401.1  (SEQ ID NO: 39) EVQLLESGGGEVQPGGSLRLSCAASGSVFSIDSMSWFRQAPGKGLELVCLITGGRTTYYAESV  KGRFTCSRDNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNADDYWGQGTLVTVKP  CDR1:  (SEQ ID NO: 120) SGSVFSIDSM  CDR2:  (SEQ ID NO: 137) LITGGRTTY  CDR3:  (SEQ ID NO: 122) NAVVSTGWGRNADDYW  H11v421  (SEQ ID NO: 40) EVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGLELVSLITGGRTTYYAESV  KGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNADDYWGQGTLVTVKP  CDR1:  (SEQ ID NO: 138) SGSVFSIDAM  CDR2:  (SEQ ID NO: 137) LITGGRTTY  CDR3:  (SEQ ID NO: 122) NAVVSTGWGRNADDYW  H11v421.1  (SEQ ID NO: 41) EVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFROAPGKGLELVCLITGGRTTYYAESV  KGRFTCSRDNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNADDYWGQGTLVTVKP  CDR1:  (SEQ ID NO: 138) SGSVFSIDAM  CDR2:  (SEQ ID NO: 137) LITGGRTTY  CDR3:  (SEQ ID NO: 122) NAVVSTGWGRNADDYW  hzC06v1.1  (SEQ ID NO: 42) EVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMGWYRQAPGKGLELVSALSGTISSATYAESV  KGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCYADVSTGWGRDAHGYWGQGTLVTV  CDR1:  (SEQ ID NO: 138) SGSVFSIDAM  CDR2:  (SEQ ID NO: 139) LSGISSAT  CDR3:  (SEQ ID NO: 116) YADVSTGWGRDAHGYW  hzCO6v1.2  (SEQ ID NO: 43) EVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMGWYRQAPGKGRELVSALSGISSATYAESV  KGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCYADVSTGWGRDAHGYWGQGTLVTV  CDR1:  (SEQ ID NO: 106) GSVFSIDAM  CDR2:  (SEQ ID NO: 139) LSGISSAT  CDR3:  (SEQ ID NO: 116) YADVSTGWGRDAHGYW  hzC06v1.3  (SEQ ID NO: 44) EVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMGWYRQAPGKQRELVSALSGISSATYAESV KGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCYADVSTFWGRDAHGYWGQGTLVTV CDR1:  (SEQ ID NO: 106) GSVFSIDAM  CDR2:  (SEQ ID NO: 139) LSGISSAT  CDR3:  (SEQ ID NO: 116) YADVSTGWGRDAHGYW  hzC06v1.4  (SEQ ID NO: 45) EVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMGWYRQAPGQQRELVSALSGISSATYAESV KGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCYADVSTGWGRDAHGYWGQGTLVTV CDR1:  (SEQ ID NO: 138) SGSVFSIDAM  CDR2:  (SEQ ID NO: 139) LSGISSAT  CDR3:  (SEQ ID NO: 140) ADVSTGWGRDAHGYW  hzC06v2.1  (SEQ ID NO: 46) EVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMGWYRQAPGKGLELVAVLSGISSATYAESV  KGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCYADVSTGWGRDAHGYWGQGTLVTV  CDR1:  (SEQ ID NO: 138) SGSVFSIDAM  CDR2:  (SEQ ID NO: 139) LSGISSAT  CDR3:  (SEQ ID NO: 116) YADVSIGWGRDAHGYW  hzC06v2.2  (SEQ ID NO: 47) EVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMGWYRQAPGKGRELVAVLSGISSATYAESV KGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCYADVSTGWGRDAHGYWGQGTLVTV CDR1:  (SEQ ID NO: 138) SGSVFSIDAM  CDR2:  (SEQ ID NO: 139) LSGISSAT CDR3:  (SEQ ID NO: 116) YADVSTGWGRDAHGYW  hzC06v2.3  (SEQ ID NO: 48) EVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMGWYRQAPGKQRELVAVLSGISSATYAESV  KGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCYADVSTGWGRDAHGYWGQGTLVTV  CDR1:  (SEQ ID NO: 138) SGSVFSIDAM  CDR2:  (SEQ ID NO: 139) LSGISSAT CDR3:  (SEQ ID NO: 116) YADVSTGWGRDAHGYW  hzC06v2.4  (SEQ ID NO: 49) EVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMGWYRQAPGQQRELVAVLSGISSATYAESV KGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCYADVSTGWGRDAHGYWGQGTLVTV CDR1:  (SEQ ID NO: 138) SGSVFSIDAM  CDR2:  (SEQ ID NO: 139) LSGISSAT  CDR3:  (SEQ ID NO: 116) YADVSTGWGRDAHGYW  hzC06v3  (SEQ ID NO: 50) EVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMGWYRQAPGKQRELVAVLSGISSAKYAESV  KGRFTISRDNAKNTLYLQMSSERAEDTAVYYCYADVSTGWGRDAHGYWGQGTLVTV  CDR1:  (SEQ ID NO: 138) SGSVFSIDAM  CDR2:  (SEQ ID NO: 141) LSGISSAK  CDR3:  (SEQ ID NO: 116) YADVSTGWGRDAHGYW  hzC06v3.1  (SEQ ID NO: 51) EVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMGWYRLAPGQQRELVAVLSGISSAKYAESV  KGRFTISRDNAKNTLYLQMSSERAEDTAVYYCYADVSTGWGRDAHGYWGQGTLVTV  CDR1:  (SEQ ID NO: 138) SGSVFSIDAM  CDR2:  (SEQ ID NO: 141) LSGISSAK  CDR3:  (SEQ ID NO: 116) YADVSTGWGRDAHGYW  hzC06v3.2  (SEQ ID NO: 52) EVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMGWYRQAPGKQRELVAVLSGISSAKYADSV KGRFTISGDNAKNTLYLQMSSLRAEDTAVYYCYADVSTGWGRDAHGYWGQGTLVTV CDR1:  (SEQ ID NO: 138) SGSVFSIDAM  CDR2:  (SEQ ID NO: 141) LSGISSAK  CDR3:  (SEQ ID NO: 116) YADVSTGWGRDAHGYW  hzC06v3.3  (SEQ ID NO: 53) EVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMGWYRQAPGKQRELVAVLSGISSAKYAESV KGRFTISRDSAKNAVYLQMDGLKPEDTAVYYCYADVSTGWGRDAHGYWGQGTLVTV CDR1:  (SEQ ID NO: 138) SGSVFSIAM  CDR2:  (SEQ ID NO: 141) LSGISSAK  CDR3:  (SEQ ID NO: 116) YADVSTGWGRDAHGYW  hzC06v3.4  (SEQ ID NO: 54) EVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMGWYRQAPGKQRELVAVLSGISSAKYAESV  KGRFTISRDNAKNTVYLQMSSLRAEDTAVYYCYADVSTGWGRDAHGYWGQGTLVTV  CDR1:  (SEQ ID NO: 138) SGSVFSIDAM  CDR2:  (SEQ ID NO: 141) LSGISSAK  CDR3:  (SEQ ID NO: 116) YADVSTGWGRDAHGYW  hzC06v3.5  (SEQ ID NO: 55)  EVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMGWYRQAPGKQRELVAYLSGISSAKYAESV  KGRFTISRASAPNTLYLQMSSLRAEDTAVYYCYADVSTGWGRDAHGYWGQGTLVTV  CDR1:  (SEQ ID NO: 138) SGSVFSIDAM  CDR2:  (SEQ ID NO: 141) LSGISSAK  CDR3:  (SEQ ID NO: 116) YADVSTGWGRDAHGYW  hzC06v3.6  (SEQ ID NO: 56) EVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMGWYRQAPGKQRELVAVLSGISSAKYAESV KGRFTISRASAPNTVYLQMSSLRAEDTAVYYCYADVSTGWGRDAHGYWGQGTLVTV CDR1:  (SEQ ID NO: 138)  SGSVFSIDAM  CDR2:  (SEQ ID NO: 141) LSGISSAK  CDR3:  (SEQ ID NO: 116) YADVSTGWGRDAHGYW  hzC06v3.7  (SEQ ID NO: 57) EVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMGWYRQAPGKQRELVAVLSGISSAKYAASA PGRFTISRDAVKNTVYLQMSSLRAEDTAVYYCYADVSTGWGRDAHGYWGQGTLVTV CDR1:  (SEQ ID NO: 138) SGSVFSIDAM  CDR2:  (SEQ ID NO: 141) LSGISSAK  CDR3:  (SEQ ID NO: 116) YADVSTGWGRDAHGYW  hzC06v3.8  (SEQ ID NO: 58) EVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMGWYRQAPGKQRELVAVLSGISSAKYAASA  PGRFTISRDAVENTVYLQMSSLRAEDTAVYYCYADVSTGWGRDAHGYWGQGTLVTV  CDR1:  (SEQ ID NO: 138) SGSVFSIDAM  CDR2:  (SEQ ID NO: 141) LSGISSAK  CDR3:  (SEQ ID NO: 116) YADVSTGWGRDAHGYW  hzC06v3.9  (SEQ ID NO: 59) EVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMGWYRQAPGKQRELVAVLSGISSAKYAASA  PGRFTISRDNAKNTVYLQMSSLRAEDTAVYYCYADVSTGWGRDAHGYWGQGTLVTV CDR1:  (SEQ ID NO: 138) SGSVFSIDAM  CDR2:  (SEQ ID NO: 141) LSGISSAK  CDR3:  (SEQ ID NO: 116) YADVSTGWGRDAHGYW  hzC06v3.10  (SEQ ID NO: 60) EVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMGWYRQAPGKQRELVAVLSGISSAKYADAV KGRFTISRASAPNTVYLQMSSLRAEDTAVYYCYADVSTGWGRDAHGYWGQGTLVTV CDR1:  (SEQ ID NO: 138) SGSVFSIDAM  CDR2:  (SEQ ID NO: 141) LSGISSAK  CDR3:  (SEQ ID NO: 142) ADVSTGWGRDAHGYW  hzC06v3.11  (SEQ ID NO: 61) EVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMGWYRQAPGKQRELVAVLSGISSAKYADAV EGRFTISRASAPNTVYLQMSSLRAEDTAVYYCYADVSTGWGRDAHGYWGQGTLVTV CDR1:  (SEQ ID NO: 138) SGSVFSIDAM  CDR2:  (SEQ ID NO: 141) LSGISSAK  CDR3:  (SEQ ID NO: 116) YADVSTGWGRDAHGYW  hzC06v3.12  (SEQ ID NO: 62) EVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMGWYRQAPGKQRELVAVLSGISSAKYAASA PGRFTISRASAPNTVYLQMSSLRAEDTAVYYCYADVSTGWGRDAHGYWGQGTLVTV  CDR1:  (SEQ ID NO: 138) SGSVFSIDAM  CDR2:  (SEQ ID NO: 141) LSGISSAK  CDR3:  (SEQ ID NO: 116) YADVSTGWGRDAHGYW  hzC04v1  (SEQ ID NO: 63) EVQLLESGGGEVQPGGSLRLSCAASGFTFSTHGMDWFRQAPGKDLEWVSAINNGGSWTSYASS  VKGRFTISRDNAKNTLYLQMSSLRAEDTAVYWCQNRVTRGQGTLVTV  CDR1:  (SEQ ID NO: 143) SGFTFSTHGM  CDR2:  (SEQ ID NO: 144) AINNGGSWTS  CDR3:  (SEQ ID NO: 145) CQNRVTR hzC04v1.2  (SEQ ID NO: 64) EVQLLESGGGEVQPGGSLRLSCAASGFTFSTHGMDWFRQAPGKDLEWVSAINNGGSWTSYASS VKGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCQNRVTRGQGTLVTV  CDR1:  (SEQ ID NO: 143) SGFTFSTHGM CDR2:  (SEQ ID NO: 144) AINNGGSWTS  CDR3:  (SEQ ID NO: 146) QNRVTR  hzC04v1.2.1  (SEQ ID NO: 65)  EVQLLESGGGEVQPGGSLRLSCAASGFTFSTHGMDWFRQAPGKDLEWVSAINGGSWTSYASS VKGFRTISRDNAKNTLYLQMSSLRAEDTAVYYCQNRVTRGQGTLVTV CDR1:  (SEQ ID NO: 143) SGFTFSTHGM  CDR2:  (SEQ ID NO: 147) INQGGSWTS  CDR3:  (SEQ ID NO: 146) QNRVTR hzC04v2  (SEQ ID NO: 66) EVQLLESGGGEVQPGGSLRLSCAASGFTFSTHGMDWFRQAPGKGLEWVSAINNGGSWTSYASS VKGRFTISRDNAKNTLYLQMSSLRAEDTAVYWCQNRVTRGQGTLVTV CDR1:  (SEQ ID NO: 143) SGFTFSTHGM CDR2:  (SEQ ID NO: 144) AINNGGSWTS  CDR3:  (SEQ ID NO: 146) QNRVTR  hzC04v2.2  (SEQ ID NO: 67) EVQLLESGGGEVQPGGSLRLSCAASGFTFSTHGMDWFRQAPGKGLEWVSAINNGGWTSYASS VKGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCQNRVTRGQGTLVTV  CDR1:  (SEQ ID NO: 143) SGFTFSTHGM  CDR2:  (SEQ ID NO: 144) AINNGGSWTS  CDR3:  (SEQ ID NO: 146) QNRVTR  hzC04v5  (SEQ ID NO: 68)  EVQLLESGGGEVQPGGSLRLSCAASGFTFSTHGMDWFRQAPGKDLEWVSAIQSGGSWTSYASS  VKGRFTISRDNAKNTLYLQMSSLRAEDTAVYWCQNRVTRGQGTLVTV  CDR1:  (SEQ ID NO: 143) SGFTFSTHGM  CDR2:  (SEQ ID NO: 147) AIQSGGSWTS  CDR3:  (SEQ ID NO: 146) QNRVTR  hzC04v5.1  (SEQ ID NO: 69) EVQLLESGGGEVQPGGSLRLSCAASGFTFSTHGMDWFRQAPGKDLEWVSAIQSGGSWTSYASS  VKGRFTISRDNAKNTLYLEMNNLKPEDTAVYWCQNRVTRGQGTLVTV  CDR1:  (SEQ ID NO: 143) SGFTFSTHGM  CDR2:  (SEQ ID NO: 147) AIQSGGSWTS  CDR3:  (SEQ ID NO: 146) QNRVTR  hzC04v5.2  (SEQ ID NO: 70) EVQLLESGGGEVQPGGSLRLSCAASGFTFSTHGMDWFRQAPGKDLEWVSAIQSGGSWTSYASS  VKGRFTISRDNAKNTLYLQMNNLRAEDTAVYWCQNRVTRGQGTLVTV CDR1:  (SEQ ID NO: 143) SGFTFSTHGM  CDR2:  (SEQ ID NO: 147) AIQSGGSWTS  CDR3:  (SEQ ID NO: 146) QNRVTR  hze04v5.3  (SEQ ID NO: 71) EVQLLESGGGEVQPGGSLRLSCAASGFTFSTHGMDWFRQAPGKDLEWVSAIQSGGSWTSYASS  VKGRFTISRDNAKNTLYLEMSSLRAEDTAVYWCQNRVTRGQGTLVTV  CDR1:  (SEQ ID NO: 143) SGFTFSTHGM  CDR2:  (SEQ ID NO: 147) AIQSGGSWTS  CDR3: (SEQ ID NO: 146) QNRVTR  hzC04v5.4  (SEQ ID NO: 72) EVQLLESGGGEVQPGGSLRLSCAASGFTFSTHGMDWFRQAPGKDLEWVSAIQSGGSWTSYASS  VKGRFTISRDNAKNTLYLQMSSLRPEDTAVYWCQNRVTRGQGTLVTV  CDR1:  (SEQ ID NO: 143) SGFTFSTHGM  CDR2:  (SEQ ID NO: 147) AIQSGGSWTS  CDR3:  (SEQ ID NO: 146) QNRVTR  hzC04v5.5  (SEQ ID NO: 73) EVQLLESGGGEVQPGGSLRLSCAASGFTFSTHGMDWFRQAPGKDLEWVSAIQSGGSWTSYASS VKGRFTISRDNAKNTLYLQMQQLRAEDTAVYWCQNRVTRGQGTLVTV CDR1:  (SEQ ID NO: 143) SGFTFSTHGM  CDR2:  (SEQ ID NO: 147) AIQSGGSWTS  CDR3:  (SEQ ID NO: 146) QNRVTR  hzC04v5.6  (SEQ ID NO: 74) EVQLLESGGGEVQPGGSLRLSCAASGFTFSTHGMDWFRQAPGKDLEWVSAIQSGGSWTSYASS VKGRFTISRDNAKNTLYLQMQNLRAEDTAVYWCQNRVTRGQGTLVTV CDR1:  (SEQ ID NO: 143) SGFTFSTHGM  CDR2:  (SEQ ID NO: 147) AIQSGGSWTS  CDR3:  (SEQ ID NO: 146) QNRVTR  hzC04v5.7  (SEQ ID NO: 75) EVQLLESGGGEVQPGGSLRLSCAASGFTFSTHGMDWFRQAPGKDLEWVSAIQSGGSWTSYASS VKGRFTISRDNAKNTLYLQMDNLRAEDTAVYWCQNRVTRGQGTLVTV CDR1:  (SEQ ID NO: 143) SGFTFSTHGM  CDR2:  (SEQ ID NO: 147) AIQSGGSWTS  CDR3:  (SEQ ID NO: 146) QNRVTR  hzC04v5.8  (SEQ ID NO: 76) EVQLLESGGGEVQPGGSLRLSCAASGFTFSTHGMDWFRQAPGKDLEWVSAIQSGGSWTSYASS VKGRFTISRDNAKNTLYLQMNDLRAEDTAVYWCQNRVTRGQGTLVTV CDR1:  (SEQ ID NO: 143) SGFTFSTHGM  CDR2:  (SEQ ID NO: 147) AIQSGGSWTS  CDR3:  (SEQ ID NO: 146) QNRVTR  hzC04v5.9  (SEQ ID NO: 77) EVQLLESGGGEVQPGGSLRLSCAASGFTFSTHGMDWFRQAPGKDLEWVSAIQSGGSWTSYASS  VKGRFTISRDNAKNTLYLQMDDLRAEDTAVYWCQNRVTRGQGTLVTV  CDR1:  (SEQ ID NO: 143) SGFTFSTHGM  CDR2:  (SEQ ID NO: 147) AIQSGGSWTS  CDR3:  (SEQ ID NO: 146) QNRVTR  hzC04v5.10  (SEQ ID NO: 78) EVQLLESGGGEVQPGGSLRLSCAASGFTFSTHGMDWFRQAPGKDLEWVSAIQSGGSWTSYASS  VKGRFTISRDNAKNTLYLQMQDLRAEDTAVYWCQNRVTRGQGTLVTV  CDR1:  (SEQ ID NO: 143) SGFTFSTHGM  CDR2:  (SEQ ID NO: 147) AIQSGGSWTS  CDR3:  (SEQ ID NO: 146) QNRVTR  hzC04v5.11  (SEQ ID NO: 79) EVQLLESGGGEVQPGGSLRLSCAASGFTFSTHGMDWFRQAPGKDLEWVSAIQSGGSWTSYASS VKGRFTISRDNAKNTLYLQMNQLRAEDTAVYCQNRVTRGQGTLVTV CDR1:  (SEQ ID NO: 143) SGFTFSTHGM  ODES:  (SEQ ID NO: 147) AIQSGGSWTS  CDR3:  (SEQ ID NO: 146) QNRVTR  hzC04v5.12  (SEQ ID NO: 80) EVQLLESGGGEVQPGGSLRLSCAASGFTFSTHGMDWFRQAPGKDLEWVSAIQSGGSWTSYASS  VKGRFTISRDNAKNTLYLQMSNLRAEDTAVYWCQNRVTRGQGTLVTV  CDR1:  (SEQ ID NO: 143) SGFTFSTHGM  CDR2:  (SEQ ID NO: 147) AIQSGGSWTS  CDR3:  (SEQ ID NO: 146) QNRVTR  2x H11v420 + Fc deletion polypeptide  (SEQ ID NO: 81) MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD DYWGQGTLVTVKPGGSGGSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKG LELVSAITGGRTTYYAESVKGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNA DDYWGQGTLVTVPGGGGDKTHTCPPCPAPGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSH EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP IEKTISKAKGQPREPQVYTLPPSRDELTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTT PPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLPGK 2x H11v420.1 + Fc deletion polypeptide  (SEQ ID NO: 82) MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD DYWGQGTLVTVKPGGSGGSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKG LELVSAITGGRTTYYAESVKGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNA DDYWGQGTLVTVPGGGGDKTHTCPPCPAPGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSH EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP IEKTISKAKGQPREPQVYTLPPSRDELTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTT PPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLPGK 2x H11v420 IgG1-Fc  (SEQ ID NO: 83) MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD DYWGQGTLVTVKPGGSGGSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKG LELVSAITGGRTTYYAESVKGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNA DDYWGQGTLVTVPGGGGDKTHTCPPCPAPGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSH EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP IEKTISKAKGQPREPQVYTLPPSRDELTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTT PPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLPGK 2x H11v420.1 IgG1-Fc  (SEQ ID NO: 84) MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD DYWGQGTLVTVKPGGSGGSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKG LELVSAITGGRTTYYAESVKGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNA DDYWGQGTLVTVPGGGGDKTHTCPPCPAPGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSH EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP IEKTISKAKGQPREPQVYTLPPSRDELTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTT PPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLPGK 2x H11v401 + Fc deletion polypeptide  (SEQ ID NO: 85)  MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD DYWGQGTLVTVKPGGSGGSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKG LELVSAITGGRTTYYAESVKGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNA DDYWGQGTLVTVPGGGGDKTHTCPPCPAPGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSH EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP IEKTISKAKGQPREPQVYTLPPSRDELTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTT PPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLPGK 2x H11v401.1 + Fc deletion polypeptide  (SEQ ID NO: 86) MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD DYWGQGTLVTVKPGGSGGSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKG LELVSAITGGRTTYYAESVKGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNA DDYWGQGTLVTVPGGGGDKTHTCPPCPAPGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSH EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP IEKTISKAKGQPREPQVYTLPPSRDELTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTT PPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLPGK 2x H11v401 IgG1-Fc  (SEQ ID NO: 87) MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD DYWGQGTLVTVKPGGSGGSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKG LELVSAITGGRTTYYAESVKGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNA DDYWGQGTLVTVPGGGGDKTHTCPPCPAPGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSH EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP IEKTISKAKGQPREPQVYTLPPSRDELTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTT PPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLPGK 2x H11v401.1 IgG1-Fc  (SEQ ID NO: 88) MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD DYWGQGTLVTVKPGGSGGSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKG LELVSAITGGRTTYYAESVKGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNA DDYWGQGTLVTVPGGGGDKTHTCPPCPAPGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSH EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP IEKTISKAKGQPREPQVYTLPPSRDELTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTT PPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLPGK 2x H11v421 + Fc deletion polypeptide  (SEQ ID NO: 89) MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD DYWGQGTLVTVKPGGSGGSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKG LELVSAITGGRTTYYAESVKGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNA DDYWGQGTLVTVPGGGGDKTHTCPPCPAPGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSH EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP IEKTISKAKGQPREPQVYTLPPSRDELTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTT PPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLPGK 2x H11v421.1 + Fc deletion polypeptide  (SEQ ID NO: 90) MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD DYWGQGTLVTVKPGGSGGSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKG LELVSAITGGRTTYYAESVKGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNA DDYWGQGTLVTVPGGGGDKTHTCPPCPAPGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSH EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP IEKTISKAKGQPREPQVYTLPPSRDELTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTT PPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLPGK 2x H11v421 IgG1-Fc  (SEQ ID NO: 91) MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD DYWGQGTLVTVKPGGSGGSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKG LELVSAITGGRTTYYAESVKGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNA DDYWGQGTLVTVPGGGGDKTHTCPPCPAPGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSH EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP IEKTISKAKGQPREPQVYTLPPSRDELTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTT PPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLPGK 2x H11v421.1 IgG1-Fc  (SEQ ID NO: 92) MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD DYWGQGTLVTVKPGGSGGSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKG LELVSAITGGRTTYYAESVKGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNA DDYWGQGTLVTVPGGGGDKTHTCPPCPAPGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSH EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP IEKTISKAKGQPREPQVYTLPPSRDELTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTT PPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLPGK 2x hzC06 IgG1-Fc  (SEQ ID NO: 93) EVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMGWYRQAPGKQRELVAVLSGISSAKYAASA PGRFTISRDNAKNTVYLQMSSLRAEDTAVYYCYADVSTGWGRDAHGYWGQGTLVTVKPGGSGG SEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMGWYRQAPGKQRELVAVLSGISSAKYAAS APGRFTISRDNAKNTVYLQMSSLRAEDTAVYYCYADVSTGWGRDAHGYWGQGTLVTVKPGGGG KKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRPEVTCVVVDVSHEDPEVKFNWYVDGVE VHNAKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPREP QVYTLPPSRDELTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVDLSDGSFFLYSK LTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK 3x H11v420 + Fc deletion polypeptide  (SEQ ID NO: 94) MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD DYWGQGTLVTVKPGGSGGSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKG LELVSAITGGRTTYYAESVKGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNA DDYWGQGTLVTVPGGGGDKTHTCPPCPAPGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSH EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP IEKTISKAKGQPREPQVYTLPPSRDELTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTT EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD 3x H11v420.1 + Fc deletion polypeptide  (SEQ ID NO: 95) MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD DYWGQGTLVTVKPGGSGGSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKG LELVSAITGGRTTYYAESVKGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNA DDYWGQGTLVTVPGGGGDKTHTCPPCPAPGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSH EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP IEKTISKAKGQPREPQVYTLPPSRDELTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTT EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD 3x H11v420 IgG1-Fc  (SEQ ID NO: 96) MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD DYWGQGTLVTVKPGGSGGSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKG LELVSAITGGRTTYYAESVKGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNA DDYWGQGTLVTVPGGGGDKTHTCPPCPAPGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSH EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP IEKTISKAKGQPREPQVYTLPPSRDELTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTT EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD 3x H11v420.1 IgG1-Fc  (SEQ ID NO: 97) MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD DYWGQGTLVTVKPGGSGGSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKG LELVSAITGGRTTYYAESVKGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNA DDYWGQGTLVTVPGGGGDKTHTCPPCPAPGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSH EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP IEKTISKAKGQPREPQVYTLPPSRDELTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTT EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD 3x H11v401 + Fc deletion polypeptide  (SEQ ID NO: 98) MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD DYWGQGTLVTVKPGGSGGSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKG LELVSAITGGRTTYYAESVKGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNA DDYWGQGTLVTVPGGGGDKTHTCPPCPAPGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSH EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP IEKTISKAKGQPREPQVYTLPPSRDELTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTT EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD 3x H11v401.1 + Fc deletion polypeptide  (SEQ ID NO: 99) MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD DYWGQGTLVTVKPGGSGGSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKG LELVSAITGGRTTYYAESVKGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNA DDYWGQGTLVTVPGGGGDKTHTCPPCPAPGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSH EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP IEKTISKAKGQPREPQVYTLPPSRDELTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTT EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD 3x H11v401 IgG1-Fc  (SEQ ID NO: 100) MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD DYWGQGTLVTVKPGGSGGSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKG LELVSAITGGRTTYYAESVKGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNA DDYWGQGTLVTVPGGGGDKTHTCPPCPAPGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSH EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP IEKTISKAKGQPREPQVYTLPPSRDELTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTT EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD 3x H11v401.1 IgG1-Fc  (SEQ ID NO: 101) MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD DYWGQGTLVTVKPGGSGGSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKG LELVSAITGGRTTYYAESVKGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNA DDYWGQGTLVTVPGGGGDKTHTCPPCPAPGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSH EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP IEKTISKAKGQPREPQVYTLPPSRDELTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTT EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD 3x H11v421 + Fc deletion polypeptide  (SEQ ID NO: 102) MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD DYWGQGTLVTVKPGGSGGSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKG LELVSAITGGRTTYYAESVKGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNA DDYWGQGTLVTVPGGGGDKTHTCPPCPAPGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSH EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP IEKTISKAKGQPREPQVYTLPPSRDELTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTT EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD 3x H11v421.1 + Fc deletion polypeptide  (SEQ ID NO: 103) MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD DYWGQGTLVTVKPGGSGGSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKG LELVSAITGGRTTYYAESVKGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNA DDYWGQGTLVTVPGGGGDKTHTCPPCPAPGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSH EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP IEKTISKAKGQPREPQVYTLPPSRDELTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTT EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD 3x H11v421 IgG1-Fc  (SEQ ID NO: 104) MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD DYWGQGTLVTVKPGGSGGSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKG LELVSAITGGRTTYYAESVKGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNA DDYWGQGTLVTVPGGGGDKTHTCPPCPAPGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSH EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP IEKTISKAKGQPREPQVYTLPPSRDELTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTT EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD 3x H11v421.1 IgG1-Fc  (SEQ ID NO: 105) MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD DYWGQGTLVTVKPGGSGGSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKG LELVSAITGGRTTYYAESVKGRFTISRDNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNA DDYWGQGTLVTVPGGGGDKTHTCPPCPAPGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSH EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP IEKTISKAKGQPREPQVYTLPPSRDELTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTT EDPEVKFNWYVDGVEVHANKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAP MKWVTFISLLFLFSSAYSEVQLLESGGGEVQPGGSLRLSCAASGSVFSIDAMSWFRQAPGKGL ELVSAITGGRTTYYAESVKGRFTISRKNAKNTLYLQMSSLRAEDTAVYYCNAVVSTGWGRNAD

In some embodiments, the fusion proteins targeting GITR of the present disclosure include two or more polypeptide sequences that are operably linked via amino acid linkers. In some embodiments, these linkers are composed predominately of the amino acids Glycine and Serine, denoted as GS-linkers herein. The GS-linkers of the fusion proteins of the present disclosure can be of various lengths, for example, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20 amino acids in length.

In some embodiments, the GS-linker comprises an amino acid sequence selected from the group consisting of GGSGGS, i.e., (GGS)₂ (SEQ ID NO: 12); GGSGGSGGS, i.e., (GGS)₃ (SEQ ID NO: 13); GGSGGSGGSGGS, i.e., (GGS)₄ (SEQ ID NO: 14); and GGSGGSGGSGGSGGS, i.e., (GGS)₅ (SEQ ID NO: 15).

In some embodiments, the linker is a flexible linker comprising Glycine residues, such as, by way of non-limiting example, GG, GGG, GGGG (SEQ ID NO: 16), GGGGG (SEQ ID NO: 17), and GGGGGG (SEQ ID NO: 18).

In some embodiments, the GITR-binding fusion protein includes a combination of a GS-linker and a Glycine linker.

In some embodiments, the multivalent GITR-targeting fusion protein is tetravalent. In some embodiments, the tetravalent GITR-targeting molecule of the disclosure includes two copies of a GITR-targeting fusion protein having the following structure: (GITR-BD)-Linker-(GITR-BD)-Linker-Hinge-Fc. In some embodiments, the tetravalent GITR-targeting molecule of the disclosure includes two copies of a GITR-binding fusion protein having the following structure: (GITR-BD)-Linker-(GITR-BD)-Linker-Hinge-Fc, where the GITR-BD is an isolated polypeptide sequence that binds GITR. In some embodiments, the tetravalent GITR-targeting molecule of the disclosure includes two copies of a GITR-binding fusion protein having the following structure: (GITR-BD)-Linker-(GITR-BD)-Linker-Hinge-Fc, where the GITR-BD is an sdAb sequence that binds GITR. In some embodiments, the tetravalent GITR-targeting molecule of the disclosure includes two copies of a GITR-binding fusion protein having the following structure: (GITR-BD)-Linker-(GITR-BD)-Linker-Hinge-Fc, where the GITR-BD is a humanized or fully human sdAb sequence that binds GITR. In some embodiments, the tetravalent GITR-targeting molecule comprises a complementarity determining region 1 (CDR1) comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 106, 109, 112, 117, 120, 125, 131, 138, 143, 148, and 149; a complementarity determining region 2 (CDR2) comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 107, 110, 113, 115, 118, 121, 123, 128, 130, 132, 134, 136, 137, 139, 141, 144, and 147; and a complementarity determining region 3 (CDR3) comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 108, 111, 114, 116, 119, 122, 124, 126, 127, 129, 133, 135, 140, 142, 145, 146, and 150. In some embodiments, the tetravalent GITR-targeting molecule contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80. In some embodiments, the tetravalent GITR-targeting molecule contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62. In some embodiments, the tetravalent GITR-targeting molecule at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80. In some embodiments, the tetravalent GITR-targeting molecule comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 81-93.

In some embodiments, the multivalent GITR-targeting fusion protein is hexavalent. In some embodiments, the hexavalent GITR-targeting molecule of the disclosure includes two copies of a GITR-targeting fusion protein having the following structure: (GITR-BD)-Linker-(GITR-BD)-Linker-(GITR-BD)-Linker-Hinge-Fc. In some embodiments, the hexavalent GITR-targeting molecule of the disclosure includes two copies of a GITR-targeting fusion protein having the following structure: (GITR-BD)-Linker-(GITR-BD)-Linker-(GITR-BD)-Linker-Hinge-Fc, where the GITR-BD is a humanized or an isolated polypeptide sequence that binds GITR. In some embodiments, the hexavalent GITR-targeting molecule of the disclosure includes two copies of a GITR-targeting fusion protein having the following structure: (GITR-BD)-Linker-(GITR-BD)-Linker-(GITR-BD)-Linker-Hinge-Fc, where the GITR-BD is an sdAb sequence that binds GITR. In some embodiments, the hexavalent GITR-targeting molecule of the disclosure includes two copies of a GITR-targeting fusion protein having the following structure: (GITR-BD)-Linker-(GITR-BD)-Linker-(GITR-BD)-Linker-Hinge-Fc, where the GITR-BD is a humanized or fully human sdAb sequence that binds GITR. In some embodiments, the hexavalent GITR-targeting molecule comprises a complementarity determining region 1 (CDR1) comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 106, 109, 112, 117, 120, 125, 131, 138, 143, 148, and 149; a complementarity determining region 2 (CDR2) comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 107, 110, 113, 115, 118, 121, 123, 128, 130, 132, 134, 136, 137, 139, 141, 144, and 147; and a complementarity determining region 3 (CDR3) comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 108, 111, 114, 116, 119, 122, 124, 126, 127, 129, 133, 135, 140, 142, 145, 146, and 150. In some embodiments, the hexavalent GITR-targeting molecule contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 19-80. In some embodiments, the hexavalent GITR-targeting molecule contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42-62. In some embodiments, the hexavalent GITR-targeting molecule contains at least one GITR-BD that comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 63-80. In some embodiments, the hexavalent GITR-targeting molecule comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 94-105.

The GITR-targeting proteins described herein are useful in a variety of therapeutic, diagnostic and prophylactic indications. For example, the GITR-targeting proteins are useful in treating a variety of diseases and disorders in a subject. In some embodiments, the GITR-targeting proteins are useful in treating, alleviating a symptom of, ameliorating and/or delaying the progression of a disease or disorder in a subject suffering from or identified as being at risk for an inflammatory disease or disorder. In some embodiments, the GITR-targeting proteins are useful in treating, alleviating a symptom of, ameliorating and/or delaying the progression of a cancer or other neoplastic condition. In some embodiments, the cancer is bladder cancer, breast cancer, uterine/cervical cancer, ovarian cancer, prostate cancer, testicular cancer, esophageal cancer, gastrointestinal cancer, pancreatic cancer, colorectal cancer, colon cancer, kidney cancer, head and neck cancer, lung cancer, stomach cancer, germ cell cancer, bone cancer, liver cancer, thyroid cancer, skin cancer, neoplasm of the central nervous system, lymphoma, leukemia, myeloma, sarcoma, and virus-related cancer. In certain embodiments, the cancer is a metastatic cancer, refractory cancer, or recurrent cancer. In some embodiments, the GITR-targeting proteins are useful in reducing or depleting the number of T regulatory cells in a tumor of a subject in need thereof. In some embodiments, the GITR-targeting proteins are useful in stimulating an immune response in a subject. In some embodiments, the GITR-targeting proteins are useful in treating, alleviating a symptom of, ameliorating and/or delaying the progression of an autoimmune disease or disorder. In some embodiments, the GITR-targeting proteins are useful in treating, alleviating a symptom of, ameliorating and/or delaying the progression of viral, bacterial and parasitic infections.

Therapeutic formulations of the disclosure, which include a GITR-targeting molecule of the disclosure, are used to treat or alleviate a symptom associated with a disease or disorder associated with aberrant activity and/or expression of GITR in a subject. A therapeutic regimen is carried out by identifying a subject, e.g., a human patient suffering from (or at risk of developing) a disease or disorder associated with aberrant activity and/or expression of GITR using standard methods, including any of a variety of clinical and/or laboratory procedures. The term patient includes human and veterinary subjects. The term subject includes humans and other mammals.

Efficaciousness of treatment is determined in association with any known method for diagnosing or treating the particular disease or disorder associated with aberrant activity and/or expression of GITR. Alleviation of one or more symptoms of the disease or disorder associated with aberrant activity and/or expression of GITR indicates that the GITR-targeting molecule confers a clinical benefit.

Therapeutic uses of the GITR-targeting molecules of the disclosure can also include the administration of one or more additional agents. In some embodiments, the one or more additional agents is an anti-GITR antibody or fusion protein, an anti-PD1 antibody or fusion protein, a LAG-3 antibody or fusion protein, a CTLA-4 antibody or fusion protein, and/or a PD-L1 antibody or fusion protein.

The GITR-targeting molecules of the present invention may be administered alone or with other modes of treatment. They may be provided before, substantially contemporaneous with, or after other modes of treatment, for example, surgery, chemotherapy, radiation therapy, or the administration of a biologic, such as another therapeutic polypeptide/antibody.

In some embodiments, the GITR-targeting molecules of the present invention may be used in combination with a chemotherapeutic agent. Examples of chemotherapeutic agents include, but are not limited to, alkylating agents such as thiotepa and Cytoxan® cyclosphosphamide; alkyl sulfonates such as busulfan, improsulfan and piposulfan; aziridines such as benzodopa, carboquone, meturedopa, and uredopa; ethylenimines and methylamelamines including altretamine, triethylenemelamine, trietylenephosphoramide, triethiylenethiophosphoramide and trimethylolomelamine; acetogenins (especially bullatacin and bullatacinone); a camptothecin (including the synthetic analogue topotecan); bryostatin; callystatin; CC-1065 (including its adozelesin, carzelesin and bizelesin synthetic analogues); cryptophycins (particularly cryptophycin 1 and cryptophycin 8); dolastatin; duocarmycin (including the synthetic analogues, KW-2189 and CB1-TM1); eleutherobin; pancratistatin; a sarcodictyin; spongistatin; nitrogen mustards such as chlorambucil, chlornaphazine, cholophosphamide, estramustine, ifosfamide, mechlorethamine, mechlorethamine oxide hydrochloride, melphalan, novembichin, phenesterine, prednimustine, trofosfamide, uracil mustard; nitrosureas such as carmustine, chlorozotocin, fotemustine, lomustine, nimustine, and ranimnustine; antibiotics such as the enediyne antibiotics (e.g., calicheamicin, especially calicheamicin gamma1I and calicheamicin omegaI1 (see. e.g., Agnew, Chem Intl. Ed. Engl., 33: 183-186 (1994)); dynemicin, including dynemicin A; bisphosphonates, such as clodronate; an esperamicin; as well as neocarzinostatin chromophore and related chromoprotein enediyne antiobiotic chromophores), aclacinomysins, actinomycin, authramycin, azaserine, bleomycins, cactinomycin, carabicin, carminomycin, carzinophilin, chromomycinis, dactinomycin, daunorubicin, detorubicin, 6-diazo-5-oxo-L-norleucine, Adriamycin® doxorubicin (including morpholino-doxorubicin, cyanomorpholino-doxorubicin, 2-pyrrolino-doxorubicin and deoxydoxorubicin), epirubicin, esorubicin, idarubicin, marcellomycin, mitomycins such as mitomycin C, mycophenolic acid, nogalamycin, olivomycins, peplomycin, potfiromycin, puromycin, quelamycin, rodorubicin, streptonigrin, streptozocin, tubercidin, ubenimex, zinostatin, zorubicin; anti-metabolites such as methotrexate and 5-fluorouracil (5-FU); folic acid analogues such as denopterin, methotrexate, pteropterin, trimetrexate; purine analogs such as fludarabine, 6-mercaptopurine, thiamiprine, thioguanine; pyrimidine analogs such as ancitabine, azacitidine, 6-azauridine, carmofur, cytarabine, dideoxyuridine, doxifluridine, enocitabine, floxuridine; androgens such as calusterone, dromostanolone propionate, epitiostanol, mepitiostane, testolactone; anti-adrenals such as aminoglutethimide, mitotane, trilostane; folic acid replenisher such as frolinic acid; aceglatone; aldophosphamide glycoside; aminolevulinic acid; eniluracil; amsacrine; bestrabucil; bisantrene; edatraxate; defofamine; demecolcine; diaziquone; elfornithine; elliptinium acetate; an epothilone; etoglucid; gallium nitrate; hydroxyurea; lentinan; lonidainine; maytansinoids such as maytansine and ansamitocins; mitoguazone; mitoxantrone; mopidanmol; nitraerine; pentostatin; phenamet; pirarubicin; losoxantrone; podophyllinic acid; 2-ethylhydrazide; procarbazine; PSK® polysaccharide complex (JHS Natural Products, Eugene, Oreg.); razoxane; rhizoxin; sizofiran; spirogermanium; tenuazonic acid; triaziquone; 2,2′,2″-trichlorotriethylamine; trichothecenes (especially T-2 toxin, verracurin A, roridin A and anguidine); urethan; vindesine; dacarbazine; mannomustine; mitobronitol; mitolactol; pipobroman; gacytosine; arabinoside (“Ara-C”); cyclophosphamide; thiotepa; taxoids, e.g., Taxol® paclitaxel (Bristol-Myers Squibb Oncology, Princeton, N.J.), Abraxane® Cremophor-free, albumin-engineered nanoparticle formulation of paclitaxel (American Pharmaceutical Partners, Schaumberg, Ill.), and Taxotere® doxetaxel (Rhône-Poulenc Rorer, Antony, France); chloranbucil; Gemzar® gemcitabine; 6-thioguanine; mercaptopurine; methotrexate; platinum analogs such as cisplatin, oxaliplatin and carboplatin; vinblastine; platinum; etoposide (VP-16); ifosfamide; mitoxantrone; vincristine; Navelbine® vinorelbine; novantrone; teniposide; edatrexate; daunomycin; aminopterin; xeloda; ibandronate; irinotecan (Camptosar, CPT-11) (including the treatment regimen of irinotecan with 5-FU and leucovorin); topoisomerase inhibitor RFS 2000; difluorometlhylornithine (DMFO); retinoids such as retinoic acid; capecitabine; combretastatin; leucovorin (LV); oxaliplatin, including the oxaliplatin treatment regimen (FOLFOX); inhibitors of PKC-alpha, Raf, H-Ras, EGFR (e.g., erlotinib (Tarceva®)) and VEGF-A that reduce cell proliferation and pharmaceutically acceptable salts, acids or derivatives of any of the above.

Further nonlimiting exemplary chemotherapeutic agents include anti-hormonal agents that act to regulate or inhibit hormone action on cancers such as anti-estrogens and selective estrogen receptor modulators (SERMs), including, for example, tamoxifen (including Nolvadex® tamoxifen), raloxifene, droloxifene, 4-hydroxytamoxifen, trioxifene, keoxifene, LY117018, onapristone, and Fareston® toremifene; aromatase inhibitors that inhibit the enzyme aromatase, which regulates estrogen production in the adrenal glands, such as, for example, 4(5)-imidazoles, aminoglutethimide, Megase® megestrol acetate, Aromasin® exemestane, formestanie, fadrozole, Rivisor® vorozole, Femara® letrozole, and Arimidex® anastrozole; and anti-androgens such as flutamide, nilutamide, bicalutamide, leuprolide, and goserelin; as well as troxacitabine (a 1,3-dioxolane nucleoside cytosine analog); antisense oligonucleotides, particularly those which inhibit expression of genes in signaling pathways implicated in abherant cell proliferation, such as, for example, PKC-alpha, Ralf and H-Ras; ribozymes such as a VEGF expression inhibitor (e.g., Angiozyme® ribozyme) and a HER2 expression inhibitor; vaccines such as gene therapy vaccines, for example, Allovectin® vaccine, Leuvectin® vaccine, and Vaxid® vaccine; Proleukin® rIL-2; Lurtotecan® topoisomerase 1 inhibitor; Abarelix® rmRH; and pharmaceutically acceptable salts, acids or derivatives of any of the above.

In some embodiments, the GITR-targeting molecule of the present invention can be used together with an anti-angiogenesis agent. The angiogenesis agent refers to a small molecular weight substance, a polynucleotide (including, e.g., an inhibitory RNA (RNAi or siRNA)), a polypeptide, an isolated protein, a recombinant protein, an antibody, or conjugates or fusion proteins thereof, that inhibits angiogenesis, vasculogenesis, or undesirable vascular permeability, either directly or indirectly. It should be understood that the anti-angiogenesis agent includes those agents that bind and block the angiogenic activity of the angiogenic factor or its receptor. For example, an anti-angiogenesis agent is an antibody or other antagonist to an angiogenic agent, e.g., antibodies to VEGF-A (e.g., bevacizumab (Avastin®)) or to the VEGF-A receptor (e.g., KDR receptor or Flt-1 receptor), anti-PDGFR inhibitors such as Gleevec® (Imatinib Mesylate), small molecules that block VEGF receptor signaling (e.g., PTK787/ZK2284, SU6668, Sutent®/SUI 1248 (sunitinib malate), AMG706, or those described in, e.g., international patent application WO 2004/113304). Anti-angiogensis agents also include native angiogenesis inhibitors, e.g., angiostatin, endostatin, etc. See, e.g., Klagsbrun and D'Amore (1991) Annu. Rev. Physiol. 53:217-39; Streit and Detmar (2003) Oncogene 22:3172-3179 (e.g., Table 3 listing anti-angiogenic therapy in malignant melanoma); Ferrara & Alitalo (1999) Nature Medicine 5(12):1359-1364; Tonini et al. (2003) Oncogene 22:6549-6556 (e.g., Table 2 listing known anti-angiogenic factors); and, Sato (2003) Int. J. Clin. Oncol. 8:200-206 (e.g., Table 1 listing anti-angiogenic agents used in clinical trials).

In some embodiments, the GITR-targeting molecule is used in combination with other anti-tumor agents, such as anti-HER-2 antibodies, anti-CD20 antibodies, an epidermal growth factor receptor (EGFR) antagonist (e.g., a tyrosine kinase inhibitor), HER1/EGFR inhibitor (e.g., erlotinib (Tarceva®), platelet derived growth factor inhibitors (e.g., Gleevec® (Imatinib Mesylate)), a COX-2 inhibitor (e.g., celecoxib), interferons, CTLA4 inhibitors (e.g., anti-CTLA antibody ipilimumab (YERVOY®)), PD-1 inhibitors (e.g., anti-PD1 antibodies, BMS-936558), PDL1 inhibitors (e.g., anti-PDL1 antibodies, MPDL3280A), PDL2 inhibitors (e.g., anti-PDL2 antibodies), cytokines, antagonists (e.g., neutralizing antibodies) that bind to one or more of the following targets ErbB2, ErbB3, ErbB4, PDGFR-beta, BlyS, APRIL, BCMA, PD-1, PDL1, PDL2, CTLA4, or VEGF receptor(s), TRAIL/Apo2, and other bioactive and organic chemical agents, etc.

In some embodiments, the GITR-targeting molecule is administered during and/or after treatment in combination with one or more additional agents. In some embodiments, the GITR-targeting molecule and the additional agent are formulated into a single therapeutic composition, and the GITR-targeting molecule and additional agent are administered simultaneously. Alternatively, the GITR-targeting molecule and additional agent are separate from each other, e.g., each is formulated into a separate therapeutic composition, and the GITR-targeting molecule and the additional agent are administered simultaneously, or the GITR-targeting molecule and the additional agent are administered at different times during a treatment regimen. For example, the GITR-targeting molecule is administered prior to the administration of the additional agent, the GITR-targeting molecule is administered subsequent to the administration of the additional agent, or the GITR-targeting molecule and the additional agent are administered in an alternating fashion. As described herein, the GITR-targeting molecule and additional agent are administered in single doses or in multiple doses.

In some embodiments, the GITR-targeting molecule and the additional agent(s) are administered simultaneously. For example, the GITR-targeting molecule and the additional agent(s) can be formulated in a single composition or administered as two or more separate compositions. In some embodiments, the GITR-targeting molecule and the additional agent(s) are administered sequentially, or the GITR-targeting molecule and the additional agent are administered at different times during a treatment regimen.

Methods for the screening of GITR-targeting molecules that possess the desired specificity include, but are not limited to, enzyme linked immunosorbent assay (ELISA), enzymatic assays, flow cytometry, and other immunologically mediated techniques known within the art.

The disclosure further provides nucleic acid sequences and particularly DNA sequences that encode the present fusion proteins. Preferably, the DNA sequence is carried by a vector suited for extrachromosomal replication such as a phage, virus, plasmid, phagemid, cosmid, YAC, or episome. In particular, a DNA vector that encodes a desired fusion protein can be used to facilitate the methods of preparing the GITR-targeting molecules described herein and to obtain significant quantities of the fusion protein. The DNA sequence can be inserted into an appropriate expression vector, i.e., a vector which contains the necessary elements for the transcription and translation of the inserted protein-coding sequence. A variety of host-vector systems may be utilized to express the protein-coding sequence. These include mammalian cell systems infected with virus (e.g., vaccinia virus, adenovirus, etc.); insect cell systems infected with virus (e.g., baculovirus); microorganisms such as yeast containing yeast vectors, or bacteria transformed with bacteriophage DNA, plasmid DNA or cosmid DNA. Depending on the host-vector system utilized, any one of a number of suitable transcription and translation elements may be used.

The disclosure also provides methods of producing a GITR-targeting molecule by culturing a cell under conditions that lead to expression of the polypeptide, wherein the cell comprises an isolated nucleic acid molecule encoding a GITR-targeting molecule described herein, and/or vectors that include these isolated nucleic acid sequences. The disclosure provides methods of producing a GITR-targeting molecule by culturing a cell under conditions that lead to expression of the GITR-targeting molecule, wherein the cell comprises an isolated nucleic acid molecule encoding a GITR-targeting molecule described herein, and/or vectors that include these isolated nucleic acid sequences.

The fusion proteins of the disclosure (also referred to herein as “active compounds”), and derivatives, fragments, analogs and homologs thereof, can be incorporated into pharmaceutical compositions suitable for administration. Such compositions typically comprise the fusion protein and a pharmaceutically acceptable carrier. As used herein, the term “pharmaceutically acceptable carrier” is intended to include any and all solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorption delaying agents, and the like, compatible with pharmaceutical administration. Suitable carriers are described in the most recent edition of Remington's Pharmaceutical Sciences, a standard reference text in the field, which is incorporated herein by reference. Suitable examples of such carriers or diluents include, but are not limited to, water, saline, ringer's solutions, dextrose solution, and 5% human serum albumin. Liposomes and non-aqueous vehicles such as fixed oils may also be used. The use of such media and agents for pharmaceutically active substances is well known in the art. Except insofar as any conventional media or agent is incompatible with the active compound, use thereof in the compositions is contemplated. Supplementary active compounds can also be incorporated into the compositions.

A pharmaceutical composition of the disclosure is formulated to be compatible with its intended route of administration. Examples of routes of administration include parenteral, e.g., intravenous, intradermal, subcutaneous, intratumoral, oral (e.g., inhalation), transdermal (i.e., topical), transmucosal, and rectal administration. Solutions or suspensions used for parenteral, intradermal, or subcutaneous application can include the following components: a sterile diluent such as water for injection, saline solution, fixed oils, polyethylene glycols, glycerine, propylene glycol or other synthetic solvents; antibacterial agents such as benzyl alcohol or methyl parabens; antioxidants such as ascorbic acid or sodium bisulfite; chelating agents such as ethylenediaminetetraacetic acid (EDTA); buffers such as acetates, citrates or phosphates, and agents for the adjustment of tonicity such as sodium chloride or dextrose. The pH can be adjusted with acids or bases, such as hydrochloric acid or sodium hydroxide. The parenteral preparation can be enclosed in ampoules, disposable syringes or multiple dose vials made of glass or plastic.

Pharmaceutical compositions suitable for injectable use include sterile aqueous solutions (where water soluble) or dispersions and sterile powders for the extemporaneous preparation of sterile injectable solutions or dispersion. For intravenous administration, suitable carriers include physiological saline, bacteriostatic water, Cremophor EL™ (BASF, Parsippany, N.J.) or phosphate buffered saline (PBS). In all cases, the composition must be sterile and should be fluid to the extent that easy syringeability exists. It must be stable under the conditions of manufacture and storage and must be preserved against the contaminating action of microorganisms such as bacteria and fungi. The carrier can be a solvent or dispersion medium containing, for example, water, ethanol, polyol (for example, glycerol, propylene glycol, and liquid polyethylene glycol, and the like), and suitable mixtures thereof. The proper fluidity can be maintained, for example, by the use of a coating such as lecithin, by the maintenance of the required particle size in the case of dispersion and by the use of surfactants. Prevention of the action of microorganisms can be achieved by various antibacterial and antifungal agents, for example, parabens, chlorobutanol, phenol, ascorbic acid, thimerosal, and the like. In many cases, it will be preferable to include isotonic agents, for example, sugars, polyalcohols such as manitol, sorbitol, sodium chloride in the composition. Prolonged absorption of the injectable compositions can be brought about by including in the composition an agent which delays absorption, for example, aluminum monostearate and gelatin.

Sterile injectable solutions can be prepared by incorporating the active compound in the required amount in an appropriate solvent with one or a combination of ingredients enumerated above, as required, followed by filtered sterilization. Generally, dispersions are prepared by incorporating the active compound into a sterile vehicle that contains a basic dispersion medium and the required other ingredients from those enumerated above. In the case of sterile powders for the preparation of sterile injectable solutions, methods of preparation are vacuum drying and freeze-drying that yields a powder of the active ingredient plus any additional desired ingredient from a previously sterile-filtered solution thereof.

Oral compositions generally include an inert diluent or an edible carrier. They can be enclosed in gelatin capsules or compressed into tablets. For the purpose of oral therapeutic administration, the active compound can be incorporated with excipients and used in the form of tablets, troches, or capsules. Oral compositions can also be prepared using a fluid carrier for use as a mouthwash, wherein the compound in the fluid carrier is applied orally and swished and expectorated or swallowed. Pharmaceutically compatible binding agents, and/or adjuvant materials can be included as part of the composition. The tablets, pills, capsules, troches and the like can contain any of the following ingredients, or compounds of a similar nature: a binder such as microcrystalline cellulose, gum tragacanth or gelatin; an excipient such as starch or lactose, a disintegrating agent such as alginic acid, Primogel, or corn starch; a lubricant such as magnesium stearate or Sterotes; a glidant such as colloidal silicon dioxide; a sweetening agent such as sucrose or saccharin; or a flavoring agent such as peppermint, methyl salicylate, or orange flavoring.

For administration by inhalation, the compounds are delivered in the form of an aerosol spray from pressured container or dispenser which contains a suitable propellant, e.g., a gas such as carbon dioxide, or a nebulizer.

Systemic administration can also be by transmucosal or transdermal means. For transmucosal or transdermal administration, penetrants appropriate to the barrier to be permeated are used in the formulation. Such penetrants are generally known in the art, and include, for example, for transmucosal administration, detergents, bile salts, and fusidic acid derivatives. Transmucosal administration can be accomplished through the use of nasal sprays or suppositories. For transdermal administration, the active compounds are formulated into ointments, salves, gels, or creams as generally known in the art.

The compounds can also be prepared in the form of suppositories (e.g., with conventional suppository bases such as cocoa butter and other glycerides) or retention enemas for rectal delivery.

In one embodiment, the active compounds are prepared with carriers that will protect the compound against rapid elimination from the body, such as a controlled release formulation, including implants and microencapsulated delivery systems. Biodegradable, biocompatible polymers can be used, such as ethylene vinyl acetate, polyanhydrides, polyglycolic acid, collagen, polyorthoesters, and polylactic acid. Methods for preparation of such formulations will be apparent to those skilled in the art. The materials can also be obtained commercially from Alza Corporation and Nova Pharmaceuticals, Inc. Liposomal suspensions can also be used as pharmaceutically acceptable carriers. These can be prepared according to methods known to those skilled in the art, for example, as described in U.S. Pat. No. 4,522,811.

It is especially advantageous to formulate oral or parenteral compositions in dosage unit form for ease of administration and uniformity of dosage. Dosage unit form as used herein refers to physically discrete units suited as unitary dosages for the subject to be treated; each unit containing a predetermined quantity of active compound calculated to produce the desired therapeutic effect in association with the required pharmaceutical carrier. The specification for the dosage unit forms of the disclosure are dictated by and directly dependent on the unique characteristics of the active compound and the particular therapeutic effect to be achieved, and the limitations inherent in the art of compounding such an active compound for the treatment of individuals.

The pharmaceutical compositions can be included in a kit, container, pack, or dispenser together with instructions for administration. These pharmaceutical compositions can be included in diagnostic kits with instructions for use.

Pharmaceutical compositions are administered in an amount effective for treatment or prophylaxis of the specific indication. The therapeutically effective amount is typically dependent on the weight of the subject being treated, his or her physical or health condition, the extensiveness of the condition to be treated, or the age of the subject being treated. In some embodiments, the pharmaceutical composition may be administered in an amount in the range of about 50 μg/kg body weight to about 50 mg/kg body weight per dose. In some embodiments, the pharmaceutical composition may be administered in an amount in the range of about 100 μg/kg body weight to about 50 mg/kg body weight per dose. In some embodiments, the pharmaceutical composition may be administered in an amount in the range of about 100 μg/kg body weight to about 20 mg/kg body weight per dose. In some embodiments, the pharmaceutical composition may be administered in an amount in the range of about 0.5 mg/kg body weight to about 20 mg/kg body weight per dose.

In some embodiments, the pharmaceutical composition may be administered in an amount in the range of about 10 mg to about 1,000 mg per dose. In some embodiments, the pharmaceutical composition may be administered in an amount in the range of about 20 mg to about 500 mg per dose. In some embodiments, the pharmaceutical composition may be administered in an amount in the range of about 20 mg to about 300 mg per dose. In some embodiments, the pharmaceutical composition may be administered in an amount in the range of about 20 mg to about 200 mg per dose.

The pharmaceutical composition may be administered as needed to subjects. In some embodiments, an effective dose of the pharmaceutical composition is administered to a subject one or more times. In various embodiments, an effective dose of the pharmaceutical composition is administered to the subject once a month, less than once a month, such as, for example, every two months, every three months, or every six months. In other embodiments, an effective dose of the pharmaceutical composition is administered more than once a month, such as, for example, every two weeks, every week, twice per week, three times per week, daily, or multiple times per day. An effective dose of the pharmaceutical composition is administered to the subject at least once. In some embodiments, the effective dose of the pharmaceutical composition may be administered multiple times, including for periods of at least a month, at least six months, or at least a year. In some embodiments, the pharmaceutical composition is administered to a subject as-needed to alleviate one or more symptoms of a condition.

Unless otherwise defined, scientific and technical terms used in connection with the present disclosure shall have the meanings that are commonly understood by those of ordinary skill in the art. Further, unless otherwise required by context, singular terms shall include pluralities and plural terms shall include the singular. Generally, nomenclatures utilized in connection with, and techniques of, cell and tissue culture, molecular biology, and protein and oligo- or polynucleotide chemistry and hybridization described herein are those well-known and commonly used in the art. Standard techniques are used for recombinant DNA, oligonucleotide synthesis, and tissue culture and transformation (e.g., electroporation, lipofection). Enzymatic reactions and purification techniques are performed according to manufacturer's specifications or as commonly accomplished in the art or as described herein. The foregoing techniques and procedures are generally performed according to conventional methods well known in the art and as described in various general and more specific references that are cited and discussed throughout the present specification. See e.g., Sambrook et al. Molecular Cloning: A Laboratory Manual (2d ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. (1989)). The nomenclatures utilized in connection with, and the laboratory procedures and techniques of, analytical chemistry, synthetic organic chemistry, and medicinal and pharmaceutical chemistry described herein are those well-known and commonly used in the art. Standard techniques are used for chemical syntheses, chemical analyses, pharmaceutical preparation, formulation, and delivery, and treatment of patients. The term patient includes human and veterinary subjects.

As utilized in accordance with the present disclosure, the following terms, unless otherwise indicated, shall be understood to have the following meanings:

As used herein, the terms “targeting fusion protein” and “antibody” can be synonyms. As used herein, the term “antibody” refers to immunoglobulin molecules and immunologically active portions of immunoglobulin (Ig) molecules, i.e., molecules that contain an antigen binding site that specifically binds (immunoreacts with) an antigen. By “specifically bind” or “immunoreacts with” “or directed against” is meant that the antibody reacts with one or more antigenic determinants of the desired antigen and does not react with other polypeptides or binds at much lower affinity (K_(d)>10⁻⁶). Antibodies include, but are not limited to, polyclonal, monoclonal, chimeric, dAb (domain antibody), single chain, Fab, Fab′ and F(ab′)₂ fragments, F_(v), scFvs, an Fab expression library, and single domain antibody (sdAb) fragments, for example V_(H)H, V_(NAR), engineered V_(H) or V_(K).

The basic antibody structural unit is known to comprise a tetramer. Each tetramer is composed of two identical pairs of polypeptide chains, each pair having one “light” (about 25 kDa) and one “heavy” chain (about 50-70 kDa). The amino-terminal portion of each chain includes a variable region of about 100 to 110 or more amino acids primarily responsible for antigen recognition. The carboxy-terminal portion of each chain defines a constant region primarily responsible for effector function. In general, antibody molecules obtained from humans relate to any of the classes IgG, IgM, IgA, IgE and IgD, which differ from one another by the nature of the heavy chain present in the molecule. Certain classes have subclasses (also known as isotypes) as well, such as IgG₁, IgG₂, and others. Furthermore, in humans, the light chain may be a kappa chain or a lambda chain.

The term “monoclonal antibody” (mAb) or “monoclonal antibody composition”, as used herein, refers to a population of antibody molecules that contain only one molecular species of antibody molecule consisting of a unique light chain gene product and a unique heavy chain gene product. In particular, the complementarity determining regions (CDRs) of the monoclonal antibody are identical in all the molecules of the population. MAbs contain an antigen binding site capable of immunoreacting with a particular epitope of the antigen characterized by a unique binding affinity for it.

The term “antigen-binding site” or “binding portion” refers to the part of the immunoglobulin molecule that participates in antigen binding. The antigen binding site is formed by amino acid residues of the N-terminal variable (“V”) regions of the heavy (“H”) and light (“L”) chains. Three highly divergent stretches within the V regions of the heavy and light chains, referred to as “hypervariable regions,” are interposed between more conserved flanking stretches known as “framework regions,” or “FRs”. Thus, the term “FR” refers to amino acid sequences which are naturally found between, and adjacent to, hypervariable regions in immunoglobulins. In an antibody molecule, the three hypervariable regions of a light chain and the three hypervariable regions of a heavy chain are disposed relative to each other in three-dimensional space to form an antigen-binding surface. The antigen-binding surface is complementary to the three-dimensional surface of a bound antigen, and the three hypervariable regions of each of the heavy and light chains are referred to as “complementarity-determining regions,” or “CDRs.” The assignment of amino acids to each domain is in accordance with the definitions of Kabat Sequences of Proteins of Immunological Interest (National Institutes of Health, Bethesda, Md. (1987 and 1991)), or Chothia & Lesk J. Mol. Biol. 196:901-917 (1987), Chothia et al. Nature 342:878-883 (1989).

The single domain antibody (sdAb) fragments portions of the fusion proteins of the present disclosure are referred to interchangeably herein as targeting polypeptides herein.

As used herein, the term “epitope” includes any protein determinant capable of specific binding to/by an immunoglobulin or fragment thereof, or a T-cell receptor. The term “epitope” includes any protein determinant capable of specific binding to/by an immunoglobulin or T-cell receptor. Epitopic determinants usually consist of chemically active surface groupings of molecules such as amino acids or sugar side chains and usually have specific three dimensional structural characteristics, as well as specific charge characteristics. An antibody is said to specifically bind an antigen when the dissociation constant is ≦1 μM; e.g., ≦100 nM, preferably ≦10 nM and more preferably ≦1 nM.

As used herein, the terms “immunological binding” and “immunological binding properties” and “specific binding” refer to the non-covalent interactions of the type which occur between an immunoglobulin molecule and an antigen for which the immunoglobulin is specific. The strength, or affinity of immunological binding interactions can be expressed in terms of the dissociation constant (K_(d)) of the interaction, wherein a smaller K_(d) represents a greater affinity. Immunological binding properties of selected polypeptides can be quantified using methods well known in the art. One such method entails measuring the rates of antigen-binding site/antigen complex formation and dissociation, wherein those rates depend on the concentrations of the complex partners, the affinity of the interaction, and geometric parameters that equally influence the rate in both directions. Thus, both the “on rate constant” (k_(on)) and the “off rate constant” (k_(off)) can be determined by calculation of the concentrations and the actual rates of association and dissociation. (See Nature 361:186-87 (1993)). The ratio of k_(off)/k_(on) enables the cancellation of all parameters not related to affinity, and is equal to the dissociation constant K_(d). (See, generally, Davies et al. (1990) Annual Rev Biochem 59:439-473). An antibody of the present disclosure is said to specifically bind to an antigen, when the equilibrium binding constant (K_(d)) is ≦1 μM, preferably ≦100 nM, more preferably ≦10 nM, and most preferably ≦100 pM to about 1 pM, as measured by assays such as radioligand binding assays, surface plasmon resonance (SPR), flow cytometry binding assay, or similar assays known to those skilled in the art.

Preferably, residue positions which are not identical differ by conservative amino acid substitutions.

Conservative amino acid substitutions refer to the interchangeability of residues having similar side chains. For example, a group of amino acids having aliphatic side chains is glycine, alanine, valine, leucine, and isoleucine; a group of amino acids having aliphatic-hydroxyl side chains is serine and threonine; a group of amino acids having amide-containing side chains is asparagine and glutamine; a group of amino acids having aromatic side chains is phenylalanine, tyrosine, and tryptophan; a group of amino acids having basic side chains is lysine, arginine, and histidine; and a group of amino acids having sulfur-containing side chains is cysteine and methionine. Suitable conservative amino acids substitution groups are: valine-leucine-isoleucine, phenylalanine-tyrosine, lysine-arginine, alanine valine, glutamic-aspartic, and asparagine-glutamine.

As discussed herein, minor variations in the amino acid sequences of antibodies or immunoglobulin molecules are contemplated as being encompassed by the present disclosure, providing that the variations in the amino acid sequence maintain at least 75%, more preferably at least 80%, 90%, 95%, and most preferably 99%. In particular, conservative amino acid replacements are contemplated. Conservative replacements are those that take place within a family of amino acids that are related in their side chains. Genetically encoded amino acids are generally divided into families: (1) acidic amino acids are aspartate, glutamate; (2) basic amino acids are lysine, arginine, histidine; (3) non-polar amino acids are alanine, valine, leucine, isoleucine, proline, phenylalanine, methionine, tryptophan, and (4) uncharged polar amino acids are glycine, asparagine, glutamine, cysteine, serine, threonine, tyrosine. The hydrophilic amino acids include arginine, asparagine, aspartate, glutamine, glutamate, histidine, lysine, serine, and threonine. The hydrophobic amino acids include alanine, cysteine, isoleucine, leucine, methionine, phenylalanine, proline, tryptophan, tyrosine and valine. Other families of amino acids include (i) serine and threonine, which are the aliphatic-hydroxy family; (ii) asparagine and glutamine, which are the amide containing family, (iii) alanine, valine, leucine and isoleucine, which are the aliphatic family; and (iv) phenylalanine, tryptophan, and tyrosine, which are the aromatic family. For example, it is reasonable to expect that an isolated replacement of a leucine with an isoleucine or valine, an aspartate with a glutamate, a threonine with a serine, or a similar replacement of an amino acid with a structurally related amino acid will not have a major effect on the binding or properties of the resulting molecule, especially if the replacement does not involve an amino acid within a framework site. Whether an amino acid change results in a functional peptide can readily be determined by assaying the specific activity of the polypeptide derivative. Assays are described in detail herein. Fragments or analogs of antibodies or immunoglobulin molecules can be readily prepared by those of ordinary skill in the art. Suitable amino- and carboxy-termini of fragments or analogs occur near boundaries of functional domains. Structural and functional domains can be identified by comparison of the nucleotide and/or amino acid sequence data to public or proprietary sequence databases. Preferably, computerized comparison methods are used to identify sequence motifs or predicted protein conformation domains that occur in other proteins of known structure and/or function. Methods to identify protein sequences that fold into a known three-dimensional structure are known. Bowie et al. Science 253:164 (1991). Thus, the foregoing examples demonstrate that those of skill in the art can recognize sequence motifs and structural conformations that may be used to define structural and functional domains in accordance with the disclosure.

Preferred amino acid substitutions are those which: (1) reduce susceptibility to proteolysis, (2) reduce susceptibility to oxidation, (3) alter binding affinity for forming protein complexes, (4) alter binding affinities, and (4) confer or modify other physicochemical or functional properties of such analogs. Analogs can include various muteins of a sequence other than the naturally-occurring peptide sequence. For example, single or multiple amino acid substitutions (preferably conservative amino acid substitutions) may be made in the naturally-occurring sequence (preferably in the portion of the polypeptide outside the domain(s) forming intermolecular contacts. A conservative amino acid substitution should not substantially change the structural characteristics of the parent sequence (e.g., a replacement amino acid should not tend to break a helix that occurs in the parent sequence, or disrupt other types of secondary structure that characterizes the parent sequence). Examples of art-recognized polypeptide secondary and tertiary structures are described in Proteins, Structures and Molecular Principles (Creighton, Ed., W. H. Freeman and Company, New York (1984)), Introduction to Protein Structure (C. Branden and J. Tooze, eds., Garland Publishing, New York, N.Y. (1991)); and Thornton et al. Nature 354:105 (1991).

The term “polypeptide fragment” as used herein refers to a polypeptide that has an amino terminal and/or carboxy-terminal deletion, but where the remaining amino acid sequence is identical to the corresponding positions in the naturally-occurring sequence deduced, for example, from a full length cDNA sequence. Fragments typically are at least 5, 6, 8 or 10 amino acids long, preferably at least 14 amino acids long’ more preferably at least 20 amino acids long, usually at least 50 amino acids long, and even more preferably at least 70 amino acids long. The term “analog” as used herein refers to polypeptides which are comprised of a segment of at least 25 amino acids that has substantial identity to a portion of a deduced amino acid sequence and which has specific binding to GITR, under suitable binding conditions. Typically, polypeptide analogs comprise a conservative amino acid substitution (or addition or deletion) with respect to the naturally-occurring sequence. Analogs typically are at least 20 amino acids long, preferably at least 50 amino acids long or longer, and can often be as long as a full-length naturally-occurring polypeptide.

Peptide analogs are commonly used in the pharmaceutical industry as non-peptide drugs with properties analogous to those of the template peptide. These types of non-peptide compound are termed “peptide mimetics” or “peptidomimetics”. Fauchere, J. Adv. Drug Res. 15:29 (1986), Veber and Freidinger TINS p. 392 (1985); and Evans et al. J. Med. Chem. 30:1229 (1987). Such compounds are often developed with the aid of computerized molecular modeling. Peptide mimetics that are structurally similar to therapeutically useful peptides may be used to produce an equivalent therapeutic or prophylactic effect. Generally, peptidomimetics are structurally similar to a paradigm polypeptide (i.e., a polypeptide that has a biochemical property or pharmacological activity), such as human antibody, but have one or more peptide linkages optionally replaced by a linkage selected from the group consisting of: —CH₂NH—, —CH₂S—, —CH₂—CH₂—, —CH═CH-(cis and trans), —COCH₂—, CH(OH)CH₂—, and —CH₂SO—, by methods well known in the art. Systematic substitution of one or more amino acids of a consensus sequence with a D-amino acid of the same type (e.g., D-lysine in place of L-lysine) may be used to generate more stable peptides. In addition, constrained peptides comprising a consensus sequence or a substantially identical consensus sequence variation may be generated by methods known in the art (Rizo and Gierasch Ann. Rev. Biochem. 61:387 (1992)); for example, by adding internal cysteine residues capable of forming intramolecular disulfide bridges which cyclize the peptide.

The term “agent” is used herein to denote a chemical compound, a mixture of chemical compounds, a biological macromolecule, and/or an extract made from biological materials.

As used herein, the terms “label” or “labeled” refers to incorporation of a detectable marker, e.g., by incorporation of a radiolabeled amino acid or attachment to a polypeptide of biotinyl moieties that can be detected by marked avidin (e.g., streptavidin containing a fluorescent marker or enzymatic activity that can be detected by optical or calorimetric methods). In certain situations, the label or marker can also be therapeutic. Various methods of labeling polypeptides and glycoproteins are known in the art and may be used. Examples of labels for polypeptides include, but are not limited to, the following: radioisotopes or radionuclides (e.g., ³H, ¹⁴C, ¹⁵N, ³⁵S, ⁹⁰Y, ⁹⁹Tc, ¹¹¹In, ¹²⁵I, ¹³¹I), fluorescent labels (e.g., FITC, rhodamine, lanthanide phosphors), enzymatic labels (e.g., horseradish peroxidase, β-galactosidase, luciferase, alkaline phosphatase), chemiluminescent, biotinyl groups, predetermined polypeptide epitopes recognized by a secondary reporter (e.g., leucine zipper pair sequences, binding sites for secondary antibodies, metal binding domains, epitope tags). In some embodiments, labels are attached by spacer arms of various lengths to reduce potential steric hindrance. The term “pharmaceutical agent or drug” as used herein refers to a chemical compound or composition capable of inducing a desired therapeutic effect when properly administered to a patient.

As used herein, the terms “treat,” treating.” “treatment,” and the like refer to reducing and/or ameliorating a disorder and/or symptoms associated therewith. By “alleviate” and/or “alleviating” is meant decrease, suppress, attenuate, diminish, arrest, and/or stabilize the development or progression of a disease such as, for example, a cancer. It will be appreciated that, although not precluded, treating a disorder or condition does not require that the disorder, condition or symptoms associated therewith be completely eliminated.

In this disclosure, “comprises,” “comprising,” “containing,” “having,” and the like can have the meaning ascribed to them in U.S. Patent law and can mean “includes,” “including,” and the like; the terms “consisting essentially of” or “consists essentially” likewise have the meaning ascribed in U.S. Patent law and these terms are open-ended, allowing for the presence of more than that which is recited so long as basic or novel characteristics of that which is recited are not changed by the presence of more than that which is recited, but excludes prior art embodiments.

By “effective amount” is meant the amount required to ameliorate the symptoms of a disease relative to an untreated patient. The effective amount of active compound(s) used to practice the present disclosure for therapeutic treatment of a disease varies depending upon the manner of administration, the age, body weight, and general health of the subject. Ultimately, the attending physician or veterinarian will decide the appropriate amount and dosage regimen. Such amount is referred to as an “effective” amount.

By “subject” is meant a mammal, including, but not limited to, a human or non-human mammal, such as a bovine, equine, canine, rodent, ovine, primate, camelid, or feline.

The term “administering,” as used herein, refers to any mode of transferring, delivering, introducing, or transporting a therapeutic agent to a subject in need of treatment with such an agent. Such modes include, but are not limited to, oral, topical, intravenous, intraperitoneal, intramuscular, intradermal, intranasal, and subcutaneous administration.

By “fragment” is meant a portion of a polypeptide or nucleic acid molecule. This portion contains, preferably, at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, or 90% of the entire length of the reference nucleic acid molecule or polypeptide. A fragment may contain 10, 20, 30, 40, 50, 60, 70, 80, 90, or 100, 200, 300, 400, 500, 600, 700, 800, 900, or 1000 nucleotides or amino acids.

Ranges provided herein are understood to be shorthand for all of the values within the range. For example, a range of 1 to 50 is understood to include any number, combination of numbers, or sub-range from the group consisting of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, or 50.

Unless specifically stated or obvious from context, as used herein, the terms “a,” “an,” and “the” are understood to be singular or plural. Unless specifically stated or obvious from context, as used herein, the term “or” is understood to be inclusive.

Unless specifically stated or obvious from context, as used herein, the term “about” is understood as within a range of normal tolerance in the art, for example within 2 standard deviations of the mean. About can be understood as within 10%, 9%, 8%, 7%, 6%, 5%, 4%, 3%, 2%, 1%, 0.5%, 0.1%, 0.05%, or 0.01% of the stated value. Unless otherwise clear from the context, all numerical values provided herein are modified by the term “about.”

The disclosure will be further described in the following examples, which do not limit the scope of the disclosure described in the claims.

EXAMPLES Example 1. GITR-Targeting Molecules Bind GITR

As shown in FIGS. 2A, 2B, and 2C, various GITR-targeting fusion proteins of the disclosure bind to GITR expressed on CHO cells as assessed by flow cytometry. The GITR antibody, TRX-518, was used as a control for these studies.

The binding affinities of the GITR-targeting molecules referred to herein as hzC06v1.1 (SEQ ID NO: 42), hzC06v1.2 (SEQ ID NO: 43), hzC06v1.3 (SEQ ID NO: 44), hzC06v1.4 (SEQ ID NO: 45), hzC06v2.1 (SEQ ID NO: 46), hzC06v2.2 (SEQ ID NO: 47), hzC06v2.3 (SEQ ID NO: 48), hzC06v2.4 (SEQ ID NO: 49), hzC06v3 (SEQ ID NO: 50), hzC06v3.1 (SEQ ID NO: 51), hzC06v3.2 (SEQ ID NO: 52), hzC06v3.3 (SEQ ID NO: 53), hzC06v3.4 (SEQ ID NO: 54), hzC06v3.5 (SEQ ID NO: 55), hzC06v3.6 (SEQ ID NO: 56), hzC06v3.7 (SEQ ID NO: 57), hzC06v3.8 (SEQ ID NO: 58), hzC06v3.9 (SEQ ID NO: 59), hzC06v3.10 (SEQ ID NO: 60), hzC06v3.11 (SEQ ID NO: 61), hzC06v3.12 (SEQ ID NO: 62), hzC04v4.1 (SEQ ID NO: 63), hzC04v4.1.2 (SEQ ID NO: 64), hzC04v4.2 (SEQ ID NO: 65), hzC04v4.2.2 (SEQ ID NO: 66), hzC04v5 (SEQ ID NO: 67), hzC04v1.2.1 (SEQ ID NO: 68), hzC04v5.1 (SEQ ID NO: 69), hzC04v5.2 (SEQ ID NO: 70), hzC04v5.3 (SEQ ID NO: 71), hzC04v5.4 (SEQ ID NO: 72), hzC04v5.5 (SEQ ID NO: 73), hzC04v5.6 (SEQ ID NO: 74), hzC04v5.7 (SEQ ID NO: 75), hzC04v5.8 (SEQ ID NO: 76), hzC04v5.9 (SEQ ID NO: 77), hzC04v5.10 (SEQ ID NO: 78), hzC04v5.11 (SEQ ID NO: 79), and hzC04v5.12 (SEQ ID NO: 80) for human and cynomolgus GITR expressed on the surface of CHO cells were determined by flow cytometry. The results are shown in FIGS. 4A-4F and 5A-5G.

Example 2. GITR-Targeting Molecules Block the Interaction Between GITR and GITR-L

As shown in FIGS. 3A, 3B, and 3C, various GITR-targeting fusion proteins of the disclosure were able to block the interaction between GITRL and GITR. Briefly, in these studies, a flow cytometry assay using GITR expressing CHO cells and recombinant GITRL was used to implement to assess blocking capacity. The GITR antibody, TRX-518, was used as a control for these studies.

Example 3. Binding Affinities of GITR-Targeting Molecules for Human and Cynomolgus GITR

The binding affinities of the GITR-targeting molecule referred to herein as bivalent hzC06v3.9-hIgG1 or 2× hzC06v3.9-IgG1 Fc (SEQ ID NO: 93) for human and cynomolgus GITR extracellular domain human IgG1 fusion protein (GITR-Fc) were determined by surface plasmon resonance. Briefly, biotinylated human and cynomolgus GITR-Fc were captured on the chip surface and then bivalent hzC06v3.9-hIgG1 was injected at 10 concentrations (0 nM-600 nM) at 40 ul/min for 120 seconds. Dissociation was followed for 240 seconds. ka1, kd1, and KD1 are reported in the table below.

GITR-Fc ka1 (1/Ms) kd1 (1/s) KD1 (nM) Cyno 1.22E+05 1.06E−02 87.1 Human 6.40E+05 4.12E−03 6.4

Example 4. Binding of GITR-Targeting Molecules for Primary Human T Cells

The ability of an anti-GITR molecule of the disclosure, referred to herein as tetravalent hzC06-hIgG1, to primary human T cells was evaluated herein. Tetravalent hzC06-hIgG1 is constructed with two copies of the GITR-binding molecule of SEQ ID NO: 93, which, in turn, is constructed with two tandem copies of a single-domain variable region (sdAb) of SEQ ID NO: 59 fused to a human IgG1 Fc domain of SEQ ID NO: 1.

Total PBMC or purified Treg isolated by fluorescence-activated cell sorting were prepared from healthy human donors. The cells were activated in vitro with anti-CD3 and anti-CD28 supplemented with recombinant human IL2. The cells were incubated with varying concentrations of tetravalent hzC06-hIgG1 and a surface phenotyping antibody cocktail. Samples were then washed and stained with a fluorescently-labeled anti-hIgG secondary antibody and then assessed by flow cytometry. Activated CD4 T cells were identified by staining with CD3, CD4, and CD25. Results of these studies are shown in FIG. 7 for activated CD4 T cells from three donors (closed symbols, solid lines) and activated Treg from two donors (open symbols, dashed lines).

Example 5. GITR-Targeting Molecules Activate NF-kB Signaling

Tetravalent anti-GITR-targeting molecules activated NF-kB signaling in reporter cell lines expressing GITR. The studies described herein used two tetravalent GITR-targeting molecules of the disclosure. The first tetravalent GITR-targeting molecule includes two copies of the GITR-binding fusion protein referred to herein as 2× hzC06v3.9 IgG1-Fc (SEQ ID NO: 93), which, in turn, includes two copies of the hzC06v3.9 GITR-BD (SEQ ID NO: 59) and the IgG1 Fc polypeptide of SEQ ID NO: 1. The second tetravalent GITR-targeting molecule includes two copies of the GITR-binding fusion protein is referred to herein as 2× C06 IgG1-Fc, which, in turn, includes two copies of the C06 GITR-BD (SEQ ID NO: 22) and the IgG1 Fc polypeptide of SEQ ID NO: 1.

HEK293 cell lines containing a NF-kB-driven secreted alkaline phosphatase (SEAP) reporter gene were stably transfected with human GITR (FIG. 8A) or cynomolgus monkey GITR (FIG. 8B). The cell lines were incubated with titrating doses of tetravalent GITR antibodies overnight at 37° C. SEAP reporter gene expression was quantified by the hydrolysis of a substrate that is measured by optical density at 650 nM.

Example 6. GITR-Targeting Molecules in Tumor Models

As shown in FIGS. 9A-9C, treatment with a GITR-targeting molecule of the disclosure significantly reduced CT26 tumor growth irrespective of day of administration. BALB/c mice were inoculated subcutaneously with CT26 colorectal carcinoma cells and were administered tetravalent C06-hIgG1, which includes two copies of the GITR-binding fusion protein referred to herein as 2× C06-IgG1 Fc, which, in turn, includes two copies of the GITR-BD of SEQ ID NO: 22 and the human IgG1 Fc polypeptide sequence of SEQ ID NO: 1) or Human IgG1-Fc as a control on Day 7 (FIG. 9A), Day 9 (FIG. 9B), or Day 11 (FIG. 9C), at which points the mean tumor volumes were 125, 230, or 310 mm³. Tetravalent C06-IgG1 Fc treatment resulted in significant reduction in tumor growth compared to Human Fc beginning 6-8 days after administration regardless of the day of treatment (p<0.05, determined via two-tailed, unpaired t-test).

As shown in FIG. 10, treatment with a GITR-targeting molecule of the disclosure produced dose-dependent suppression of CT26 tumor growth. BALB/c mice were inoculated subcutaneously with CT26 colorectal carcinoma cells and were administered tetravalent C06-mIgG2a, which includes two copies of the GITR-binding fusion protein referred to herein as 2× C06-mIgG1 2a Fc, which, in turn, includes two copies of the GITR-BD of SEQ ID NO: 22 and a murine IgG2a sequence or non-specific mIgG2a as a control on Day 9 (approximate tumor volume 260 mm³). Tetravalent C06-mIgG2a treatment resulted in significant reduction in tumor volume compared to control when administered at 2.5, 0.25, 0.08, or 0.025 mg/kg (p<0.05). Tetravalent C06-mIgG2a dosed at 0.008 mg/kg did not significantly suppress CT26 tumor growth. Statistical significance was determined via one-way ANOVA with multiple comparisons of the Tetravalent C06-mIgG2a groups to mIgG2a.

As shown in FIGS. 11A-11B, treatment with a GITR-targeting molecule of the disclosure produced dose-dependent suppression of MC38 tumor growth. C57BL/6 mice were inoculated subcutaneously with MC38 colorectal carcinoma cells and were administered tetravalent C06-mIgG2a or non-specific mIgG2a as a control on Day 7 (mean tumor volume 110-115 mm³). Administration of tetravalent C06-mIgG2a at doses of 0.08 or above resulted in significant tumor growth reduction compared to mIgG2a control beginning on Day 14 (p<0.05) (FIG. 11A). Tetravalent C06-mIgG2a treatment at 0.025 significantly reduced tumor growth compared to mIgG2a control beginning on Day 18 (p<0.05). Tetravalent C06-mIgG2a dosed at 0.008 mg/kg did not significantly suppress MC38 tumor growth. Statistical significance was determined via one-way ANOVA with multiple comparisons of the C06 groups to IgG2a. Individual tumor volumes on Day 20 after MC38 inoculation are shown in FIG. 11B. There is a similar reduction in tumor growth at this timepoint in the 2.5, 0.25, and 0.08 mg/kg treatment groups.

Example 7. Impact of Fc Function on Inhibition of CT26 Tumor Growth

BALB/c mice were inoculated subcutaneously with CT26 colorectal carcinoma cells and were administered tetravalent C06-mIgG2a with either wild-type Fc or N297G mutation to block binding to Fc receptors (mIgG2a-silent) on Day 9 (mean tumor volume 260 mm³). Non-specific mIgG2a, anti-GITR mAb1-mIgG2a, and anti-GITR control mAb1-mIgG2a-silent were used as controls. As shown in FIG. 12A, although tetravalent C06 was most potent with wild-type Fc, both wild-type and silent formats significantly reduced tumor growth compared to control (p<0.05). mAb1 only inhibited CT26 growth when administered in the wild-type Fc format. Statistical significance was determined via one-way ANOVA with multiple comparisons of the treatment groups to mIgG2a. Individual tumor volumes on Day 22 after CT26 inoculation are shown in FIG. 12B. The difference in tumor growth between Fc wild-type and silent formats of tetravalent C06 is not significant, while format was significant for the ability of mAb1 to suppress tumor growth. Kaplan-Meier analysis shows that treatment with tetravalent C06 with wild-type Fc can significantly enhance the survival of CT26-bearing mice (FIG. 12C). A single administration of tetravalent C06-mIgG2a on Day 10 extends median survival to 66 days, compared to 20 days for the mIgG2a control group.

Example 8. Treatment with GITR-Targeting Molecules Results in Resistance to Re-Challenge

Mice that had received tetravalent C06-mIgG2a-induced CT26 rejection were resistant to re-challenge. BALB/c mice that had rejected CT26 tumors upon treatment with tetravalent C06-mIgG2a were re-inoculated with CT26, Renca, or EMT6 murine tumor cell lines. As shown in FIG. 13A, mice that have previously rejected CT26 were completely resistant to tumor growth upon subsequent re-inoculation of this model. Importantly, naïve, age-matched mice demonstrated CT26 tumor growth. As shown in FIG. 13B, Renca tumors did not grow well in mice that had previously rejected CT26. Indeed, two of four mice were completely resistant, and one mouse had marked reduction in Renca growth compared to naïve, age-matched controls. Renca shares T cell epitopes with CT26, suggesting that T cell-mediated immunity is induced. As shown in FIG. 13C, EMT6 tumors grow well in BALB/c mice whether they previously eliminated CT26 upon C06 treatment or were naïve. EMT6 does not share T cell epitopes with CT26.

Example 9. Effect of Treatment with GITR-Targeting Molecules on T Cells

Treatment significantly reduced T_(reg) frequency and altered the ratio to T_(effector) cells within the tumor microenvironment. BALB/c mice were inoculated subcutaneously with CT26 colorectal carcinoma cells and were administered 2.5 mg/kg tetravalent C06-mIgG2a with either wild-type Fc or N297G mutation to block binding to Fc receptors (mIgG2a-silent) on Day 9. Non-specific mIgG2a was used as a control. Peripheral blood and tumors were collected and analyzed by flow cytometry 3 days after treatment. As shown in FIG. 14A, treatment with tetravalent C06-mIgG2a significantly reduced the frequency of circulating T_(reg), conventional CD4 T cells (4Tcon), and CD8 T cells (8T) (p<0.05). No effect was observed with the mIgG2a-silent format. As shown in FIG. 14B, treatment with tetravalent C06-mIgG2a significantly reduced the frequency of intratumoral T_(reg) and conventional CD4 T cells (p<0.001), but CD8 T cells were not changed. No effect was observed with the mIgG2a-silent format. As shown in FIG. 14C, as a consequence of the potent reduction of T_(reg) by tetravalent C06-mIgG2a, the ratios of effector T cells to T_(reg) were significantly increased in the tumor (p<0.05). Statistical significance was determined via two-tailed, unpaired t-test.

Example 10. Effect of GITR-Targeting Molecules on T Cell Activation and Proliferation

Treatment significantly induced CD8 T cell activation and proliferation. BALB/c mice were inoculated subcutaneously with CT26 colorectal carcinoma cells and were administered 2.5 mg/kg tetravalent C06-mIgG2a with either wild-type Fc or N297G mutation to block binding to Fc receptors (mIgG2a-silent) on Day 9. Non-specific mIgG2a was used as a control. Peripheral blood was analyzed by flow cytometry 12 days after treatment. As shown in FIG. 15A, treatment with tetravalent C06-mIgG2a significantly induced the frequency of circulating CD8 T cells (p<0.005), but T_(reg) and conventional CD4 T cells were not changed. This effect was not observed with the mIgG2a-silent format. As shown in FIG. 15B, CD8 T cells also adopted an activated, proliferating phenotype (CD62L⁻ Ki67⁺) following treatment with tetravalent C06-mIgG2a. Statistical significance was determined via two-tailed, unpaired t-test. 

What is claimed is:
 1. A polypeptide comprising at least two copies of a GITR-binding domain (GITR-BD), wherein the GITR-BD comprises a complementarity determining region 1 (CDR1) comprising the amino acid sequence of SEQ ID NO: 138; a complementarity determining region 2 (CDR2) comprising the amino acid sequence of SEQ ID NO: 141; and a complementarity determining region 3 (CDR3) comprising the amino acid sequence of SEQ ID NO: 116, and wherein the polypeptide does not comprise a binding domain that binds to an antigen other than GITR.
 2. The polypeptide of claim 1, wherein the GITR-BD comprises the amino acid sequence of SEQ ID NO:
 59. 3. The polypeptide of claim 2, wherein the polypeptide comprises the amino acid sequence of SEQ ID NO:
 93. 4. A tetravalent GITR-targeting molecule comprising two copies of a fusion protein comprising the structure: (GITR-BD)-Linker-(GITR-BD)-Linker-Hinge-Fc, wherein (a) each GITR-BD is a GITR-binding domain comprising a complementarity determining region 1 (CDR1) comprising the amino acid sequence of SEQ ID NO: 138; a complementarity determining region 2 (CDR2) comprising the amino acid sequence of SEQ ID NO: 141; and a complementarity determining region 3 (CDR3) comprising the amino acid sequence of SEQ ID NO: 116; (b) Linker is a linker polypeptide; (c) Hinge is a polypeptide derived from an immunoglobulin hinge region; and (d) Fc is an immunoglobulin Fc region polypeptide; and wherein the tetravalent GITR-targeting molecule does not comprise a binding domain that binds to an antigen other than GITR.
 5. The tetravalent GITR-targeting molecule of claim 4, wherein the Fc comprises an amino acid sequence selected from SEQ ID NO: 1-6.
 6. The tetravalent GITR-targeting molecule of claim 5, wherein the Hinge comprises the amino acid sequence of SEQ ID NO:
 8. 7. The tetravalent GITR-targeting molecule of claim 6, wherein each Linker comprises an amino acid sequence independently selected from SEQ ID NO: 12 and SEQ ID NO:
 16. 8. The tetravalent GITR-targeting molecule of claim 4, wherein each GITR-BD comprises the amino acid sequence of SEQ ID NO:
 59. 9. The tetravalent GITR-targeting molecule of claim 8, wherein the Fc comprises the amino acid sequence of SEQ ID NO:
 1. 10. The tetravalent GITR-targeting molecule of claim 9, wherein the Hinge comprises the amino acid sequence of SEQ ID NO:
 8. 11. The tetravalent GITR-targeting molecule of claim 10, wherein each Linker comprises an amino acid sequence independently selected from SEQ ID NO: 12 and SEQ ID NO:
 16. 12. A tetravalent GITR-targeting molecule comprising two copies of the polypeptide of claim
 3. 13. A pharmaceutical composition comprising the tetravalent GITR-targeting molecule of claim
 4. 14. A method of treating cancer comprising administering to a subject a therapeutically effective amount of the pharmaceutical composition of claim
 13. 15. The method of claim 14, wherein the cancer is selected from the group consisting of bladder cancer, breast cancer, uterine cancer, cervical cancer, ovarian cancer, prostate cancer, testicular cancer, esophageal cancer, gastrointestinal cancer, pancreatic cancer, colorectal cancer, colon cancer, kidney cancer, head and neck cancer, lung cancer, stomach cancer, germ cell cancer, bone cancer, liver cancer, thyroid cancer, skin cancer, neoplasm of the central nervous system, lymphoma, leukemia, myeloma, sarcoma, and virus-related cancer.
 16. The method of claim 15, wherein the cancer is selected from the group consisting of lung cancer, head and neck cancer, pancreatic cancer, kidney cancer, ovarian cancer, neoplasm of the central nervous system, skin cancer, and thyroid cancer.
 17. The method of claim 14, further comprising administering an anti-PD1 or anti-PDL1 antibody.
 18. The method of claim 17, wherein an anti-PD1 antibody is administered.
 19. The method of claim 18, wherein the anti-PD1 antibody is BMS-936558.
 20. A pharmaceutical composition comprising the tetravalent GITR-targeting molecule of claim
 12. 21. A method of treating cancer comprising administering to a subject a therapeutically effective amount of the pharmaceutical composition of claim
 20. 22. The method of claim 21, wherein the cancer is selected from the group consisting of bladder cancer, breast cancer, uterine cancer, cervical cancer, ovarian cancer, prostate cancer, testicular cancer, esophageal cancer, gastrointestinal cancer, pancreatic cancer, colorectal cancer, colon cancer, kidney cancer, head and neck cancer, lung cancer, stomach cancer, germ cell cancer, bone cancer, liver cancer, thyroid cancer, skin cancer, neoplasm of the central nervous system, lymphoma, leukemia, myeloma, sarcoma, and virus-related cancer.
 23. The method of claim 22, wherein the cancer is selected from the group consisting of lung cancer, head and neck cancer, pancreatic cancer, kidney cancer, ovarian cancer, neoplasm of the central nervous system, skin cancer, and thyroid cancer.
 24. The method of claim 23, further comprising administering an anti-PD1 or anti-PDL1 antibody.
 25. The method of claim 24, wherein an anti-PD1 antibody is administered.
 26. The method of claim 25, wherein the anti-PD1 antibody is BMS-936558.
 27. The polypeptide of claim 1, wherein the GITR-BD comprises an amino acid sequence selected from SEQ ID NOs: 50-59 and 61-62.
 28. The polypeptide of claim 4, wherein each GITR-BD comprises an amino acid sequence selected from SEQ ID NOs: 50-59 and 61-62. 